Canonical Allele Identifier: CA1918895766

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71815099G= , CM000672.2:g.71815099G=	GRCh38
NC_000010.10:g.73574856G= , CM000672.1:g.73574856G=	GRCh37
NC_000010.9:g.73244862G=	NCBI36
NG_008835.1:g.423153G=
NG_009301.1:g.41227C=

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.9886G= MANE Select	NP_071407.4:p.Asp3296=
ENST00000224721.12:c.9886G= MANE Select	ENSP00000224721.9:p.Asp3296=
NM_001171933.1:c.3166G=	NP_001165404.1:p.Asp1056=
NM_001171934.1:c.3061G=	NP_001165405.1:p.Asp1021=
NM_001171935.1:c.577G=	NP_001165406.1:p.Asp193=
NM_001171936.1:c.472G=	NP_001165407.1:p.Asp158=
NM_022124.5:c.9886G=	NP_071407.4:p.Asp3296=
ENST00000224721.10:c.9901G=	ENSP00000224721.8:p.Asp3301=
ENST00000398788.4:c.3166G=	ENSP00000381768.3:p.Asp1056=
ENST00000475158.1:n.3317G=
ENST00000619887.4:c.3061G=	ENSP00000478374.1:p.Asp1021=
ENST00000622827.4:c.9886G=	ENSP00000483211.1:p.Asp3296=
ENST00000642965.1:c.3819G=	ENSP00000495222.1:n.3819G=
ENST00000647092.1:c.3378G=	ENSP00000495176.1:n.3378G=
XM_006717940.2:c.10081G=	XP_006718003.1:p.Asp3361=
XM_006717942.2:c.10015G=	XP_006718005.1:p.Asp3339=
XM_011540039.1:c.10078G=	XP_011538341.1:p.Asp3360=
XM_011540040.1:c.10075G=	XP_011538342.1:p.Asp3359=
XM_011540041.1:c.10021G=	XP_011538343.1:p.Asp3341=
XM_011540042.1:c.9991G=	XP_011538344.1:p.Asp3331=
XM_011540043.1:c.9976G=	XP_011538345.1:p.Asp3326=
XM_011540044.1:c.9946G=	XP_011538346.1:p.Asp3316=
XM_011540046.1:c.9541G=	XP_011538348.1:p.Asp3181=
XM_011540047.1:c.8899G=	XP_011538349.1:p.Asp2967=
XM_011540052.1:c.6409G=	XP_011538354.1:p.Asp2137=