Canonical Allele Identifier: CA1918880418

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802983C= , CM000672.2:g.71802983C=	GRCh38
NC_000010.10:g.73562740C= , CM000672.1:g.73562740C=	GRCh37
NC_000010.9:g.73232746C=	NCBI36
NG_008835.1:g.411037C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7568C= MANE Select	ENSP00000224721.9:p.Pro2523=
ENST00000642965.1:c.1501C=	ENSP00000495222.1:n.1501C=
ENST00000647092.1:c.1165C=	ENSP00000495176.1:n.1165C=
ENST00000224721.10:c.7583C=	ENSP00000224721.8:p.Pro2528=
ENST00000398788.4:c.848C=	ENSP00000381768.3:p.Pro283=
ENST00000475158.1:n.1104C=
ENST00000619887.4:c.848C=	ENSP00000478374.1:p.Pro283=
ENST00000622827.4:c.7568C=	ENSP00000483211.1:p.Pro2523=
NM_001171933.1:c.848C=	NP_001165404.1:p.Pro283=
NM_001171934.1:c.848C=	NP_001165405.1:p.Pro283=
NM_022124.5:c.7568C=	NP_071407.4:p.Pro2523=
XM_006717940.2:c.7763C=	XP_006718003.1:p.Pro2588=
XM_006717942.2:c.7697C=	XP_006718005.1:p.Pro2566=
XM_011540039.1:c.7760C=	XP_011538341.1:p.Pro2587=
XM_011540040.1:c.7757C=	XP_011538342.1:p.Pro2586=
XM_011540041.1:c.7703C=	XP_011538343.1:p.Pro2568=
XM_011540042.1:c.7673C=	XP_011538344.1:p.Pro2558=
XM_011540043.1:c.7763C=	XP_011538345.1:p.Pro2588=
XM_011540044.1:c.7628C=	XP_011538346.1:p.Pro2543=
XM_011540045.1:c.7763C=	XP_011538347.1:p.Pro2588=
XM_011540046.1:c.7223C=	XP_011538348.1:p.Pro2408=
XM_011540047.1:c.6581C=	XP_011538349.1:p.Pro2194=
XM_011540052.1:c.4091C=	XP_011538354.1:p.Pro1364=
NM_022124.6:c.7568C= MANE Select	NP_071407.4:p.Pro2523=