Canonical Allele Identifier: CA1918878427

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798401T= , CM000672.2:g.71798401T=	GRCh38
NC_000010.10:g.73558158T= , CM000672.1:g.73558158T=	GRCh37
NC_000010.9:g.73228164T=	NCBI36
NG_008835.1:g.406455T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6877T= MANE Select	ENSP00000224721.9:p.Phe2293=
ENST00000642965.1:c.810T=	ENSP00000495222.1:n.810T=
ENST00000647092.1:c.474T=	ENSP00000495176.1:n.474T=
ENST00000224721.10:c.6892T=	ENSP00000224721.8:p.Phe2298=
ENST00000398788.4:c.157T=	ENSP00000381768.3:p.Phe53=
ENST00000475158.1:n.413T=
ENST00000619887.4:c.157T=	ENSP00000478374.1:p.Phe53=
ENST00000622827.4:c.6877T=	ENSP00000483211.1:p.Phe2293=
NM_001171933.1:c.157T=	NP_001165404.1:p.Phe53=
NM_001171934.1:c.157T=	NP_001165405.1:p.Phe53=
NM_022124.5:c.6877T=	NP_071407.4:p.Phe2293=
XM_006717940.2:c.7072T=	XP_006718003.1:p.Phe2358=
XM_006717942.2:c.7006T=	XP_006718005.1:p.Phe2336=
XM_011540039.1:c.7069T=	XP_011538341.1:p.Phe2357=
XM_011540040.1:c.7066T=	XP_011538342.1:p.Phe2356=
XM_011540041.1:c.7012T=	XP_011538343.1:p.Phe2338=
XM_011540042.1:c.6982T=	XP_011538344.1:p.Phe2328=
XM_011540043.1:c.7072T=	XP_011538345.1:p.Phe2358=
XM_011540044.1:c.6937T=	XP_011538346.1:p.Phe2313=
XM_011540045.1:c.7072T=	XP_011538347.1:p.Phe2358=
XM_011540046.1:c.6532T=	XP_011538348.1:p.Phe2178=
XM_011540047.1:c.5890T=	XP_011538349.1:p.Phe1964=
XM_011540052.1:c.3400T=	XP_011538354.1:p.Phe1134=
NM_022124.6:c.6877T= MANE Select	NP_071407.4:p.Phe2293=