Canonical Allele Identifier: CA2126957508
Gene: COCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.30885510G= , CM000676.2:g.30885510G= GRCh38
NC_000014.8:g.31354716G= , CM000676.1:g.31354716G= GRCh37
NC_000014.7:g.30424467G= NCBI36
NG_008211.2:g.15976G=

Transcript Alleles

HGVS Amino-acid change
ENST00000216361.9:c.1045G= ENSP00000216361.5:p.Glu349=
ENST00000396618.9:c.850G= MANE Select ENSP00000379862.3:p.Glu284=
ENST00000555117.2:c.907G= ENSP00000493569.1:p.Glu303=
ENST00000643575.1:c.850G= ENSP00000494838.1:p.Glu284=
ENST00000643697.1:n.1152G=
ENST00000644874.2:c.850G= ENSP00000496360.1:p.Glu284=
ENST00000216361.8:c.850G= ENSP00000216361.4:p.Glu284=
ENST00000396618.7:c.850G= ENSP00000379862.3:p.Glu284=
ENST00000460581.6:c.514G= ENSP00000451713.1:p.Glu172=
ENST00000468826.2:c.501G=
ENST00000475087.5:c.850G= ENSP00000451528.1:p.Glu284=
ENST00000555881.5:c.496G= ENSP00000452569.1:p.Glu166=
ENST00000557065.1:c.632G= ENSP00000451629.1:n.632G=
NM_001135058.1:c.850G= NP_001128530.1:p.Glu284=
NM_004086.2:c.850G= NP_004077.1:p.Glu284=
NR_038356.1:n.1355C=
XM_011536539.1:c.850G= XP_011534841.1:p.Glu284=
NM_001347720.1:c.1045G= NP_001334649.1:p.Glu349=
XM_017021071.1:c.1045G= XP_016876560.1:p.Glu349=
XM_024449506.1:c.907G= XP_024305274.1:p.Glu303=
NM_004086.3:c.850G= MANE Select NP_004077.1:p.Glu284=
NM_001135058.2:c.850G= NP_001128530.1:p.Glu284=
NM_001347720.2:c.1045G= NP_001334649.1:p.Glu349=