Canonical Allele Identifier: CA2126958567

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30886082G= , CM000676.2:g.30886082G=	GRCh38
NC_000014.8:g.31355288G= , CM000676.1:g.31355288G=	GRCh37
NC_000014.7:g.30425039G=	NCBI36
NG_008211.2:g.16548G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1442G=	ENSP00000216361.5:p.Arg481=
ENST00000396618.9:c.1247G= MANE Select	ENSP00000379862.3:p.Arg416=
ENST00000555117.2:c.1304G=	ENSP00000493569.1:p.Arg435=
ENST00000643575.1:c.1247G=	ENSP00000494838.1:p.Arg416=
ENST00000643697.1:n.1549G=
ENST00000644874.2:c.1247G=	ENSP00000496360.1:p.Arg416=
ENST00000216361.8:c.1247G=	ENSP00000216361.4:p.Arg416=
ENST00000396618.7:c.1247G=	ENSP00000379862.3:p.Arg416=
ENST00000460581.6:c.911G=	ENSP00000451713.1:p.Arg304=
ENST00000468826.2:c.898G=
ENST00000475087.5:c.1247G=	ENSP00000451528.1:p.Arg416=
NM_001135058.1:c.1247G=	NP_001128530.1:p.Arg416=
NM_004086.2:c.1247G=	NP_004077.1:p.Arg416=
NR_038356.1:n.783C=
XM_011536539.1:c.1247G=	XP_011534841.1:p.Arg416=
NM_001347720.1:c.1442G=	NP_001334649.1:p.Arg481=
XM_017021071.1:c.1442G=	XP_016876560.1:p.Arg481=
XM_024449506.1:c.1304G=	XP_024305274.1:p.Arg435=
NM_004086.3:c.1247G= MANE Select	NP_004077.1:p.Arg416=
NM_001135058.2:c.1247G=	NP_001128530.1:p.Arg416=
NM_001347720.2:c.1442G=	NP_001334649.1:p.Arg481=