Canonical Allele Identifier: CA1918878926

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799556A= , CM000672.2:g.71799556A=	GRCh38
NC_000010.10:g.73559313A= , CM000672.1:g.73559313A=	GRCh37
NC_000010.9:g.73229319A=	NCBI36
NG_008835.1:g.407610A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7289A= MANE Select	ENSP00000224721.9:p.Asp2430=
ENST00000642965.1:c.1222A=	ENSP00000495222.1:n.1222A=
ENST00000647092.1:c.886A=	ENSP00000495176.1:n.886A=
ENST00000224721.10:c.7304A=	ENSP00000224721.8:p.Asp2435=
ENST00000398788.4:c.569A=	ENSP00000381768.3:p.Asp190=
ENST00000475158.1:n.825A=
ENST00000619887.4:c.569A=	ENSP00000478374.1:p.Asp190=
ENST00000622827.4:c.7289A=	ENSP00000483211.1:p.Asp2430=
NM_001171933.1:c.569A=	NP_001165404.1:p.Asp190=
NM_001171934.1:c.569A=	NP_001165405.1:p.Asp190=
NM_022124.5:c.7289A=	NP_071407.4:p.Asp2430=
XM_006717940.2:c.7484A=	XP_006718003.1:p.Asp2495=
XM_006717942.2:c.7418A=	XP_006718005.1:p.Asp2473=
XM_011540039.1:c.7481A=	XP_011538341.1:p.Asp2494=
XM_011540040.1:c.7478A=	XP_011538342.1:p.Asp2493=
XM_011540041.1:c.7424A=	XP_011538343.1:p.Asp2475=
XM_011540042.1:c.7394A=	XP_011538344.1:p.Asp2465=
XM_011540043.1:c.7484A=	XP_011538345.1:p.Asp2495=
XM_011540044.1:c.7349A=	XP_011538346.1:p.Asp2450=
XM_011540045.1:c.7484A=	XP_011538347.1:p.Asp2495=
XM_011540046.1:c.6944A=	XP_011538348.1:p.Asp2315=
XM_011540047.1:c.6302A=	XP_011538349.1:p.Asp2101=
XM_011540052.1:c.3812A=	XP_011538354.1:p.Asp1271=
NM_022124.6:c.7289A= MANE Select	NP_071407.4:p.Asp2430=