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Human (GRCh37.p13)
Description

methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria [Source:HGNC Symbol;Acc:25221]

Gene Synonyms

C2orf25, CL25022, cblD

About this transcript

This transcript has 2 exons, is associated with 502 variant alleles and maps to 70 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000428879.1MMADHC-0011726296aaENSP00000389060.1
 
Protein coding
CCDS2189Q9H3L0 -Ensembl CanonicalGENCODE basic
ENST00000422782.2MMADHC-0041462330aaENSP00000408331.2
 
Protein coding
F8WEC0 -GENCODE basic
ENST00000303319.5MMADHC-0061436296aaENSP00000301920.5
 
Protein coding
CCDS2189Q9H3L0 NM_015702.2GENCODE basic
ENST00000460311.1MMADHC-005324No protein-
 
Processed transcript
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Statistics

Exons: 2, Coding exons: 0, Transcript length: 324 bps,

Version

ENST00000460311.1

Type

Processed transcript

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000332314 (version 1)