Canonical Allele Identifier: CA2126960933

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30889777G= , CM000676.2:g.30889777G=	GRCh38
NC_000014.8:g.31358983G= , CM000676.1:g.31358983G=	GRCh37
NC_000014.7:g.30428734G=	NCBI36
NG_008211.2:g.20243G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1834G=	ENSP00000216361.5:p.Glu612=
ENST00000396618.9:c.1639G= MANE Select	ENSP00000379862.3:p.Glu547=
ENST00000555117.2:c.1534+3465G=	ENSP00000493569.1:n.1534+3465G=
ENST00000643575.1:c.1639G=	ENSP00000494838.1:p.Glu547=
ENST00000643697.1:n.1941G=
ENST00000644874.2:c.1639G=	ENSP00000496360.1:p.Glu547=
ENST00000216361.8:c.1639G=	ENSP00000216361.4:p.Glu547=
ENST00000396618.7:c.1639G=	ENSP00000379862.3:p.Glu547=
ENST00000460581.6:c.1303G=	ENSP00000451713.1:p.Glu435=
ENST00000468826.2:c.1290G=
ENST00000475087.5:c.1477+3465G=	ENSP00000451528.1:n.1477+3465G=
NM_001135058.1:c.1639G=	NP_001128530.1:p.Glu547=
NM_004086.2:c.1639G=	NP_004077.1:p.Glu547=
NR_038356.1:n.32C=
XM_011536539.1:c.1639G=	XP_011534841.1:p.Glu547=
NM_001347720.1:c.1834G=	NP_001334649.1:p.Glu612=
XM_017021071.1:c.1834G=	XP_016876560.1:p.Glu612=
XM_024449506.1:c.1696G=	XP_024305274.1:p.Glu566=
NM_004086.3:c.1639G= MANE Select	NP_004077.1:p.Glu547=
NM_001135058.2:c.1639G=	NP_001128530.1:p.Glu547=
NM_001347720.2:c.1834G=	NP_001334649.1:p.Glu612=