Canonical Allele Identifier: CA389348546

Gene: COCH

Linked Data

• MyVariant Identifiers: chr14:g.31355264C>A (hg19) ; chr14:g.30886058C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.30886058C>A , CM000676.2:g.30886058C>A	GRCh38
NC_000014.8:g.31355264C>A , CM000676.1:g.31355264C>A	GRCh37
NC_000014.7:g.30425015C>A	NCBI36
NG_008211.2:g.16524C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216361.9:c.1418C>A	ENSP00000216361.5:p.Ala473Asp
ENST00000396618.9:c.1223C>A MANE Select	ENSP00000379862.3:p.Ala408Asp
ENST00000555117.2:c.1280C>A	ENSP00000493569.1:p.Ala427Asp
ENST00000643575.1:c.1223C>A	ENSP00000494838.1:p.Ala408Asp
ENST00000643697.1:n.1525C>A
ENST00000644874.2:c.1223C>A	ENSP00000496360.1:p.Ala408Asp
ENST00000216361.8:c.1223C>A	ENSP00000216361.4:p.Ala408Asp
ENST00000396618.7:c.1223C>A	ENSP00000379862.3:p.Ala408Asp
ENST00000460581.6:c.887C>A	ENSP00000451713.1:p.Ala296Asp
ENST00000468826.2:c.874C>A
ENST00000475087.5:c.1223C>A	ENSP00000451528.1:p.Ala408Asp
NM_001135058.1:c.1223C>A	NP_001128530.1:p.Ala408Asp
NM_004086.2:c.1223C>A	NP_004077.1:p.Ala408Asp
NR_038356.1:n.807G>T
XM_011536539.1:c.1223C>A	XP_011534841.1:p.Ala408Asp
NM_001347720.1:c.1418C>A	NP_001334649.1:p.Ala473Asp
XM_017021071.1:c.1418C>A	XP_016876560.1:p.Ala473Asp
XM_024449506.1:c.1280C>A	XP_024305274.1:p.Ala427Asp
NM_004086.3:c.1223C>A MANE Select	NP_004077.1:p.Ala408Asp
NM_001135058.2:c.1223C>A	NP_001128530.1:p.Ala408Asp
NM_001347720.2:c.1418C>A	NP_001334649.1:p.Ala473Asp