Canonical Allele Identifier: CA470282508

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73569632C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71809875C>A , CM000672.2:g.71809875C>A	GRCh38
NC_000010.10:g.73569632C>A , CM000672.1:g.73569632C>A	GRCh37
NC_000010.9:g.73239638C>A	NCBI36
NG_008835.1:g.417929C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8778C>A MANE Select	ENSP00000224721.9:p.Gly2926=
ENST00000642965.1:c.2711C>A	ENSP00000495222.1:n.2711C>A
ENST00000647092.1:c.2375C>A	ENSP00000495176.1:n.2375C>A
ENST00000224721.10:c.8793C>A	ENSP00000224721.8:p.Gly2931=
ENST00000398788.4:c.2058C>A	ENSP00000381768.3:p.Gly686=
ENST00000475158.1:n.2314C>A
ENST00000619887.4:c.2058C>A	ENSP00000478374.1:p.Gly686=
ENST00000622827.4:c.8778C>A	ENSP00000483211.1:p.Gly2926=
NM_001171933.1:c.2058C>A	NP_001165404.1:p.Gly686=
NM_001171934.1:c.2058C>A	NP_001165405.1:p.Gly686=
NM_022124.5:c.8778C>A	NP_071407.4:p.Gly2926=
XM_006717940.2:c.8973C>A	XP_006718003.1:p.Gly2991=
XM_006717942.2:c.8907C>A	XP_006718005.1:p.Gly2969=
XM_011540039.1:c.8970C>A	XP_011538341.1:p.Gly2990=
XM_011540040.1:c.8967C>A	XP_011538342.1:p.Gly2989=
XM_011540041.1:c.8913C>A	XP_011538343.1:p.Gly2971=
XM_011540042.1:c.8883C>A	XP_011538344.1:p.Gly2961=
XM_011540043.1:c.8973C>A	XP_011538345.1:p.Gly2991=
XM_011540044.1:c.8838C>A	XP_011538346.1:p.Gly2946=
XM_011540045.1:c.8973C>A	XP_011538347.1:p.Gly2991=
XM_011540046.1:c.8433C>A	XP_011538348.1:p.Gly2811=
XM_011540047.1:c.7791C>A	XP_011538349.1:p.Gly2597=
XM_011540052.1:c.5301C>A	XP_011538354.1:p.Gly1767=
NM_022124.6:c.8778C>A MANE Select	NP_071407.4:p.Gly2926=