Canonical Allele Identifier: CA470062077

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558250T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798493T>G , CM000672.2:g.71798493T>G	GRCh38
NC_000010.10:g.73558250T>G , CM000672.1:g.73558250T>G	GRCh37
NC_000010.9:g.73228256T>G	NCBI36
NG_008835.1:g.406547T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6969T>G MANE Select	ENSP00000224721.9:p.Pro2323=
ENST00000642965.1:c.902T>G	ENSP00000495222.1:n.902T>G
ENST00000647092.1:c.566T>G	ENSP00000495176.1:n.566T>G
ENST00000224721.10:c.6984T>G	ENSP00000224721.8:p.Pro2328=
ENST00000398788.4:c.249T>G	ENSP00000381768.3:p.Pro83=
ENST00000475158.1:n.505T>G
ENST00000619887.4:c.249T>G	ENSP00000478374.1:p.Pro83=
ENST00000622827.4:c.6969T>G	ENSP00000483211.1:p.Pro2323=
NM_001171933.1:c.249T>G	NP_001165404.1:p.Pro83=
NM_001171934.1:c.249T>G	NP_001165405.1:p.Pro83=
NM_022124.5:c.6969T>G	NP_071407.4:p.Pro2323=
XM_006717940.2:c.7164T>G	XP_006718003.1:p.Pro2388=
XM_006717942.2:c.7098T>G	XP_006718005.1:p.Pro2366=
XM_011540039.1:c.7161T>G	XP_011538341.1:p.Pro2387=
XM_011540040.1:c.7158T>G	XP_011538342.1:p.Pro2386=
XM_011540041.1:c.7104T>G	XP_011538343.1:p.Pro2368=
XM_011540042.1:c.7074T>G	XP_011538344.1:p.Pro2358=
XM_011540043.1:c.7164T>G	XP_011538345.1:p.Pro2388=
XM_011540044.1:c.7029T>G	XP_011538346.1:p.Pro2343=
XM_011540045.1:c.7164T>G	XP_011538347.1:p.Pro2388=
XM_011540046.1:c.6624T>G	XP_011538348.1:p.Pro2208=
XM_011540047.1:c.5982T>G	XP_011538349.1:p.Pro1994=
XM_011540052.1:c.3492T>G	XP_011538354.1:p.Pro1164=
NM_022124.6:c.6969T>G MANE Select	NP_071407.4:p.Pro2323=