Canonical Allele Identifier: CA2126957390
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30885409A= , CM000676.2:g.30885409A= GRCh38
NC_000014.8:g.31354615A= , CM000676.1:g.31354615A= GRCh37
NC_000014.7:g.30424366A= NCBI36
NG_008211.2:g.15875A=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.944A= ENSP00000216361.5:p.His315=
ENST00000396618.9:c.749A= MANE Select ENSP00000379862.3:p.His250=
ENST00000555117.2:c.806A= ENSP00000493569.1:p.His269=
ENST00000643575.1:c.749A= ENSP00000494838.1:p.His250=
ENST00000643697.1:n.1051A=
ENST00000644874.2:c.749A= ENSP00000496360.1:p.His250=
ENST00000216361.8:c.749A= ENSP00000216361.4:p.His250=
ENST00000396618.7:c.749A= ENSP00000379862.3:p.His250=
ENST00000460581.6:c.413A= ENSP00000451713.1:p.His138=
ENST00000468826.2:c.400A=
ENST00000475087.5:c.749A= ENSP00000451528.1:p.His250=
ENST00000555881.5:c.395A= ENSP00000452569.1:p.His132=
ENST00000557065.1:c.531A= ENSP00000451629.1:n.531A=
NM_001135058.1:c.749A= NP_001128530.1:p.His250=
NM_004086.2:c.749A= NP_004077.1:p.His250=
NR_038356.1:n.1452+4T=
XM_011536539.1:c.749A= XP_011534841.1:p.His250=
NM_001347720.1:c.944A= NP_001334649.1:p.His315=
XM_017021071.1:c.944A= XP_016876560.1:p.His315=
XM_024449506.1:c.806A= XP_024305274.1:p.His269=
NM_004086.3:c.749A= MANE Select NP_004077.1:p.His250=
NM_001135058.2:c.749A= NP_001128530.1:p.His250=
NM_001347720.2:c.944A= NP_001334649.1:p.His315=