Human (GRCh38.p14)
Description

DMRT like family C2 [Source:HGNC Symbol;Acc:HGNC:13911]

Location
About this transcript

This transcript has 7 exons, is associated with 3734 variant alleles and maps to 391 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000269945.8DMRTC2-2011805367aaENSP00000269945.2
 
Protein coding
CCDS33034Q8IXT2-1 NM_001040283.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000596827.5DMRTC2-2041675418aaENSP00000469525.1
 
Protein coding
B4DX56 -GENCODE basicTSL:2
ENST00000596660.1DMRTC2-203566161aaENSP00000470553.1
 
Protein coding
M0QZH7 -TSL:4CDS 3' incomplete
ENST00000600017.5DMRTC2-206559165aaENSP00000472488.1
 
Protein coding
M0R2D7 -TSL:4CDS 3' incomplete
ENST00000596258.5DMRTC2-202556134aaENSP00000472215.1
 
Protein coding
M0R1Z9 -TSL:4CDS 3' incomplete
ENST00000601660.5DMRTC2-2073076224aaENSP00000472159.1
 
Nonsense mediated decay
Q8IXT2-2 -TSL:2
ENST00000602098.1DMRTC2-208567No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000599022.1DMRTC2-205522No protein-
 
Retained intron
--TSL:3

Protein domains for ENSP00000472159.1