Canonical Allele Identifier: CA470062483

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562738G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802981G>A , CM000672.2:g.71802981G>A	GRCh38
NC_000010.10:g.73562738G>A , CM000672.1:g.73562738G>A	GRCh37
NC_000010.9:g.73232744G>A	NCBI36
NG_008835.1:g.411035G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7566G>A MANE Select	ENSP00000224721.9:p.Glu2522=
ENST00000642965.1:c.1499G>A	ENSP00000495222.1:n.1499G>A
ENST00000647092.1:c.1163G>A	ENSP00000495176.1:n.1163G>A
ENST00000224721.10:c.7581G>A	ENSP00000224721.8:p.Glu2527=
ENST00000398788.4:c.846G>A	ENSP00000381768.3:p.Glu282=
ENST00000475158.1:n.1102G>A
ENST00000619887.4:c.846G>A	ENSP00000478374.1:p.Glu282=
ENST00000622827.4:c.7566G>A	ENSP00000483211.1:p.Glu2522=
NM_001171933.1:c.846G>A	NP_001165404.1:p.Glu282=
NM_001171934.1:c.846G>A	NP_001165405.1:p.Glu282=
NM_022124.5:c.7566G>A	NP_071407.4:p.Glu2522=
XM_006717940.2:c.7761G>A	XP_006718003.1:p.Glu2587=
XM_006717942.2:c.7695G>A	XP_006718005.1:p.Glu2565=
XM_011540039.1:c.7758G>A	XP_011538341.1:p.Glu2586=
XM_011540040.1:c.7755G>A	XP_011538342.1:p.Glu2585=
XM_011540041.1:c.7701G>A	XP_011538343.1:p.Glu2567=
XM_011540042.1:c.7671G>A	XP_011538344.1:p.Glu2557=
XM_011540043.1:c.7761G>A	XP_011538345.1:p.Glu2587=
XM_011540044.1:c.7626G>A	XP_011538346.1:p.Glu2542=
XM_011540045.1:c.7761G>A	XP_011538347.1:p.Glu2587=
XM_011540046.1:c.7221G>A	XP_011538348.1:p.Glu2407=
XM_011540047.1:c.6579G>A	XP_011538349.1:p.Glu2193=
XM_011540052.1:c.4089G>A	XP_011538354.1:p.Glu1363=
NM_022124.6:c.7566G>A MANE Select	NP_071407.4:p.Glu2522=