Human (GRCh37.p13)
Description

alpha thalassemia/mental retardation syndrome X-linked [Source:HGNC Symbol;Acc:886]

Gene Synonyms

ATR2, JMS, MRXHF1, RAD54, RAD54L, SFM1, SHS, XH2, XNP, ZNF-HX

Location
About this transcript

This transcript has 34 exons, is annotated with 49 domains and features, is associated with 98622 variant alleles and maps to 1639 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000373344.5ATRX-001111672492aaENSP00000362441.4
 
Protein coding
CCDS14434B4DLE1 P46100 NM_000489.3GENCODE basic
ENST00000395603.3ATRX-002110312454aaENSP00000378967.3
 
Protein coding
CCDS14435B4DLE1 P46100 NM_138270.2GENCODE basic
ENST00000400866.2ATRX-007692160aaENSP00000383663.2
 
Protein coding
Q5JX93 -CDS 5' incomplete
ENST00000373341.1ATRX-004589126aaENSP00000362438.1
 
Protein coding
Q5H9A3 -GENCODE basic
ENST00000480283.1ATRX-00311268No protein-
 
Processed transcript
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ENST00000460639.1ATRX-006424No protein-
 
Processed transcript
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ENST00000479487.1ATRX-008408No protein-
 
Processed transcript
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ENST00000493470.1ATRX-005341No protein-
 
Processed transcript
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Statistics

Exons: 34, Coding exons: 34, Transcript length: 11,031 bps, Translation length: 2,454 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P46100

CCDS

This transcript is a member of the Human CCDS set: CCDS14435

Version

ENST00000395603.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000058861 (version 2)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.