Human (GRCh37.p13)
Description

Fanconi anemia, complementation group M [Source:HGNC Symbol;Acc:23168]

Gene Synonyms

FAAP250, KIAA1596

Location
About this transcript

This transcript has 2 exons, is associated with 734 variant alleles and maps to 262 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000267430.5FANCM-00171112048aaENSP00000267430.5
 
Protein coding
CCDS32070Q8IYD8 NM_020937.2GENCODE basic
ENST00000542564.2FANCM-00361672022aaENSP00000442493.2
 
Protein coding
B2RTQ9 -GENCODE basic
ENST00000556250.1FANCM-00455771564aaENSP00000452033.1
 
Protein coding
H0YJS3 -CDS 5' incomplete
ENST00000554809.1FANCM-00531121016aaENSP00000450632.1
 
Protein coding
--CDS 5' incomplete
ENST00000556036.1FANCM-0022354669aaENSP00000450596.1
 
Protein coding
Q8IYD8 -GENCODE basic
ENST00000555484.1FANCM-009448106aaENSP00000450797.1
 
Protein coding
H0YJ45 -CDS 5' incomplete
ENST00000557110.1FANCM-010638135aaENSP00000451846.1
 
Nonsense mediated decay
H0YJN7 -CDS 5' incomplete
ENST00000555013.1FANCM-007573No protein-
 
Processed transcript
---
ENST00000554030.1FANCM-006917No protein-
 
Retained intron
---
ENST00000553551.1FANCM-008603No protein-
 
Retained intron
---
Statistics

Exons: 2, Coding exons: 0, Transcript length: 603 bps,

Version

ENST00000553551.1

Type

Retained intron

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:
OTTHUMT00000410482 (version 1)