Canonical Allele Identifier: CA470062046

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558226C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798469C>A , CM000672.2:g.71798469C>A	GRCh38
NC_000010.10:g.73558226C>A , CM000672.1:g.73558226C>A	GRCh37
NC_000010.9:g.73228232C>A	NCBI36
NG_008835.1:g.406523C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6945C>A MANE Select	ENSP00000224721.9:p.Leu2315=
ENST00000642965.1:c.878C>A	ENSP00000495222.1:n.878C>A
ENST00000647092.1:c.542C>A	ENSP00000495176.1:n.542C>A
ENST00000224721.10:c.6960C>A	ENSP00000224721.8:p.Leu2320=
ENST00000398788.4:c.225C>A	ENSP00000381768.3:p.Leu75=
ENST00000475158.1:n.481C>A
ENST00000619887.4:c.225C>A	ENSP00000478374.1:p.Leu75=
ENST00000622827.4:c.6945C>A	ENSP00000483211.1:p.Leu2315=
NM_001171933.1:c.225C>A	NP_001165404.1:p.Leu75=
NM_001171934.1:c.225C>A	NP_001165405.1:p.Leu75=
NM_022124.5:c.6945C>A	NP_071407.4:p.Leu2315=
XM_006717940.2:c.7140C>A	XP_006718003.1:p.Leu2380=
XM_006717942.2:c.7074C>A	XP_006718005.1:p.Leu2358=
XM_011540039.1:c.7137C>A	XP_011538341.1:p.Leu2379=
XM_011540040.1:c.7134C>A	XP_011538342.1:p.Leu2378=
XM_011540041.1:c.7080C>A	XP_011538343.1:p.Leu2360=
XM_011540042.1:c.7050C>A	XP_011538344.1:p.Leu2350=
XM_011540043.1:c.7140C>A	XP_011538345.1:p.Leu2380=
XM_011540044.1:c.7005C>A	XP_011538346.1:p.Leu2335=
XM_011540045.1:c.7140C>A	XP_011538347.1:p.Leu2380=
XM_011540046.1:c.6600C>A	XP_011538348.1:p.Leu2200=
XM_011540047.1:c.5958C>A	XP_011538349.1:p.Leu1986=
XM_011540052.1:c.3468C>A	XP_011538354.1:p.Leu1156=
NM_022124.6:c.6945C>A MANE Select	NP_071407.4:p.Leu2315=