Canonical Allele Identifier: CA2126960962

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30889798C= , CM000676.2:g.30889798C=	GRCh38
NC_000014.8:g.31359004C= , CM000676.1:g.31359004C=	GRCh37
NC_000014.7:g.30428755C=	NCBI36
NG_008211.2:g.20264C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.*7C=	ENSP00000216361.5:n.*7C=
ENST00000396618.9:c.*7C= MANE Select	ENSP00000379862.3:n.*7C=
ENST00000555117.2:c.1534+3486C=	ENSP00000493569.1:n.1534+3486C=
ENST00000643575.1:c.*2+5C=	ENSP00000494838.1:n.*2+5C=
ENST00000643697.1:n.1962C=
ENST00000644874.2:c.*7C=	ENSP00000496360.1:n.*7C=
ENST00000216361.8:c.*7C=	ENSP00000216361.4:n.*7C=
ENST00000396618.7:c.*7C=	ENSP00000379862.3:n.*7C=
ENST00000460581.6:c.*7C=	ENSP00000451713.1:n.*7C=
ENST00000468826.2:c.1311C=
ENST00000475087.5:c.1477+3486C=	ENSP00000451528.1:n.1477+3486C=
NM_001135058.1:c.*7C=	NP_001128530.1:n.*7C=
NM_004086.2:c.*7C=	NP_004077.1:n.*7C=
NR_038356.1:n.11G=
XM_011536539.1:c.*2+5C=	XP_011534841.1:n.*2+5C=
NM_001347720.1:c.*7C=	NP_001334649.1:n.*7C=
XM_017021071.1:c.*7C=	XP_016876560.1:n.*7C=
XM_024449506.1:c.*7C=	XP_024305274.1:n.*7C=
NM_004086.3:c.*7C= MANE Select	NP_004077.1:n.*7C=
NM_001135058.2:c.*7C=	NP_001128530.1:n.*7C=
NM_001347720.2:c.*7C=	NP_001334649.1:n.*7C=