Canonical Allele Identifier: CA1918886462

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807523C= , CM000672.2:g.71807523C=	GRCh38
NC_000010.10:g.73567280C= , CM000672.1:g.73567280C=	GRCh37
NC_000010.9:g.73237286C=	NCBI36
NG_008835.1:g.415577C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8316C= MANE Select	ENSP00000224721.9:p.Asn2772=
ENST00000642965.1:c.2249C=	ENSP00000495222.1:n.2249C=
ENST00000647092.1:c.1913C=	ENSP00000495176.1:n.1913C=
ENST00000224721.10:c.8331C=	ENSP00000224721.8:p.Asn2777=
ENST00000398788.4:c.1596C=	ENSP00000381768.3:p.Asn532=
ENST00000475158.1:n.1852C=
ENST00000619887.4:c.1596C=	ENSP00000478374.1:p.Asn532=
ENST00000622827.4:c.8316C=	ENSP00000483211.1:p.Asn2772=
NM_001171933.1:c.1596C=	NP_001165404.1:p.Asn532=
NM_001171934.1:c.1596C=	NP_001165405.1:p.Asn532=
NM_022124.5:c.8316C=	NP_071407.4:p.Asn2772=
XM_006717940.2:c.8511C=	XP_006718003.1:p.Asn2837=
XM_006717942.2:c.8445C=	XP_006718005.1:p.Asn2815=
XM_011540039.1:c.8508C=	XP_011538341.1:p.Asn2836=
XM_011540040.1:c.8505C=	XP_011538342.1:p.Asn2835=
XM_011540041.1:c.8451C=	XP_011538343.1:p.Asn2817=
XM_011540042.1:c.8421C=	XP_011538344.1:p.Asn2807=
XM_011540043.1:c.8511C=	XP_011538345.1:p.Asn2837=
XM_011540044.1:c.8376C=	XP_011538346.1:p.Asn2792=
XM_011540045.1:c.8511C=	XP_011538347.1:p.Asn2837=
XM_011540046.1:c.7971C=	XP_011538348.1:p.Asn2657=
XM_011540047.1:c.7329C=	XP_011538349.1:p.Asn2443=
XM_011540052.1:c.4839C=	XP_011538354.1:p.Asn1613=
NM_022124.6:c.8316C= MANE Select	NP_071407.4:p.Asn2772=