Canonical Allele Identifier: CA1918878497

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798546C= , CM000672.2:g.71798546C=	GRCh38
NC_000010.10:g.73558303C= , CM000672.1:g.73558303C=	GRCh37
NC_000010.9:g.73228309C=	NCBI36
NG_008835.1:g.406600C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7022C= MANE Select	ENSP00000224721.9:p.Pro2341=
ENST00000642965.1:c.955C=	ENSP00000495222.1:n.955C=
ENST00000647092.1:c.619C=	ENSP00000495176.1:n.619C=
ENST00000224721.10:c.7037C=	ENSP00000224721.8:p.Pro2346=
ENST00000398788.4:c.302C=	ENSP00000381768.3:p.Pro101=
ENST00000475158.1:n.558C=
ENST00000619887.4:c.302C=	ENSP00000478374.1:p.Pro101=
ENST00000622827.4:c.7022C=	ENSP00000483211.1:p.Pro2341=
NM_001171933.1:c.302C=	NP_001165404.1:p.Pro101=
NM_001171934.1:c.302C=	NP_001165405.1:p.Pro101=
NM_022124.5:c.7022C=	NP_071407.4:p.Pro2341=
XM_006717940.2:c.7217C=	XP_006718003.1:p.Pro2406=
XM_006717942.2:c.7151C=	XP_006718005.1:p.Pro2384=
XM_011540039.1:c.7214C=	XP_011538341.1:p.Pro2405=
XM_011540040.1:c.7211C=	XP_011538342.1:p.Pro2404=
XM_011540041.1:c.7157C=	XP_011538343.1:p.Pro2386=
XM_011540042.1:c.7127C=	XP_011538344.1:p.Pro2376=
XM_011540043.1:c.7217C=	XP_011538345.1:p.Pro2406=
XM_011540044.1:c.7082C=	XP_011538346.1:p.Pro2361=
XM_011540045.1:c.7217C=	XP_011538347.1:p.Pro2406=
XM_011540046.1:c.6677C=	XP_011538348.1:p.Pro2226=
XM_011540047.1:c.6035C=	XP_011538349.1:p.Pro2012=
XM_011540052.1:c.3545C=	XP_011538354.1:p.Pro1182=
NM_022124.6:c.7022C= MANE Select	NP_071407.4:p.Pro2341=