Canonical Allele Identifier: CA2126957393
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30885412C= , CM000676.2:g.30885412C= GRCh38
NC_000014.8:g.31354618C= , CM000676.1:g.31354618C= GRCh37
NC_000014.7:g.30424369C= NCBI36
NG_008211.2:g.15878C=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.947C= ENSP00000216361.5:p.Thr316=
ENST00000396618.9:c.752C= MANE Select ENSP00000379862.3:p.Thr251=
ENST00000555117.2:c.809C= ENSP00000493569.1:p.Thr270=
ENST00000643575.1:c.752C= ENSP00000494838.1:p.Thr251=
ENST00000643697.1:n.1054C=
ENST00000644874.2:c.752C= ENSP00000496360.1:p.Thr251=
ENST00000216361.8:c.752C= ENSP00000216361.4:p.Thr251=
ENST00000396618.7:c.752C= ENSP00000379862.3:p.Thr251=
ENST00000460581.6:c.416C= ENSP00000451713.1:p.Thr139=
ENST00000468826.2:c.403C=
ENST00000475087.5:c.752C= ENSP00000451528.1:p.Thr251=
ENST00000555881.5:c.398C= ENSP00000452569.1:p.Thr133=
ENST00000557065.1:c.534C= ENSP00000451629.1:n.534C=
NM_001135058.1:c.752C= NP_001128530.1:p.Thr251=
NM_004086.2:c.752C= NP_004077.1:p.Thr251=
NR_038356.1:n.1452+1G=
XM_011536539.1:c.752C= XP_011534841.1:p.Thr251=
NM_001347720.1:c.947C= NP_001334649.1:p.Thr316=
XM_017021071.1:c.947C= XP_016876560.1:p.Thr316=
XM_024449506.1:c.809C= XP_024305274.1:p.Thr270=
NM_004086.3:c.752C= MANE Select NP_004077.1:p.Thr251=
NM_001135058.2:c.752C= NP_001128530.1:p.Thr251=
NM_001347720.2:c.947C= NP_001334649.1:p.Thr316=