Canonical Allele Identifier: CA2126961309

Gene: COCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30890212G= , CM000676.2:g.30890212G=	GRCh38
NC_000014.8:g.31359418G= , CM000676.1:g.31359418G=	GRCh37
NC_000014.7:g.30429169G=	NCBI36
NG_008211.2:g.20678G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396618.9:c.*421G= MANE Select	ENSP00000379862.3:n.*421G=
ENST00000555117.2:c.1534+3900G=	ENSP00000493569.1:n.1534+3900G=
ENST00000643575.1:c.*2+419G=	ENSP00000494838.1:n.*2+419G=
ENST00000644874.2:c.*421G=	ENSP00000496360.1:n.*421G=
ENST00000396618.7:c.*421G=	ENSP00000379862.3:n.*421G=
ENST00000460581.6:c.*421G=	ENSP00000451713.1:n.*421G=
ENST00000468826.2:c.1725G=
ENST00000475087.5:c.1477+3900G=	ENSP00000451528.1:n.1477+3900G=
NM_001135058.1:c.*421G=	NP_001128530.1:n.*421G=
NM_004086.2:c.*421G=	NP_004077.1:n.*421G=
XM_011536539.1:c.*2+419G=	XP_011534841.1:n.*2+419G=
NM_001347720.1:c.*421G=	NP_001334649.1:n.*421G=
XM_017021071.1:c.*421G=	XP_016876560.1:n.*421G=
XM_024449506.1:c.*421G=	XP_024305274.1:n.*421G=
NM_004086.3:c.*421G= MANE Select	NP_004077.1:n.*421G=
NM_001135058.2:c.*421G=	NP_001128530.1:n.*421G=
NM_001347720.2:c.*421G=	NP_001334649.1:n.*421G=