Canonical Allele Identifier: CA1918880449

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803049C= , CM000672.2:g.71803049C=	GRCh38
NC_000010.10:g.73562806C= , CM000672.1:g.73562806C=	GRCh37
NC_000010.9:g.73232812C=	NCBI36
NG_008835.1:g.411103C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7634C= MANE Select	ENSP00000224721.9:p.Thr2545=
ENST00000642965.1:c.1567C=	ENSP00000495222.1:n.1567C=
ENST00000647092.1:c.1231C=	ENSP00000495176.1:n.1231C=
ENST00000224721.10:c.7649C=	ENSP00000224721.8:p.Thr2550=
ENST00000398788.4:c.914C=	ENSP00000381768.3:p.Thr305=
ENST00000475158.1:n.1170C=
ENST00000619887.4:c.914C=	ENSP00000478374.1:p.Thr305=
ENST00000622827.4:c.7634C=	ENSP00000483211.1:p.Thr2545=
NM_001171933.1:c.914C=	NP_001165404.1:p.Thr305=
NM_001171934.1:c.914C=	NP_001165405.1:p.Thr305=
NM_022124.5:c.7634C=	NP_071407.4:p.Thr2545=
XM_006717940.2:c.7829C=	XP_006718003.1:p.Thr2610=
XM_006717942.2:c.7763C=	XP_006718005.1:p.Thr2588=
XM_011540039.1:c.7826C=	XP_011538341.1:p.Thr2609=
XM_011540040.1:c.7823C=	XP_011538342.1:p.Thr2608=
XM_011540041.1:c.7769C=	XP_011538343.1:p.Thr2590=
XM_011540042.1:c.7739C=	XP_011538344.1:p.Thr2580=
XM_011540043.1:c.7829C=	XP_011538345.1:p.Thr2610=
XM_011540044.1:c.7694C=	XP_011538346.1:p.Thr2565=
XM_011540045.1:c.7829C=	XP_011538347.1:p.Thr2610=
XM_011540046.1:c.7289C=	XP_011538348.1:p.Thr2430=
XM_011540047.1:c.6647C=	XP_011538349.1:p.Thr2216=
XM_011540052.1:c.4157C=	XP_011538354.1:p.Thr1386=
NM_022124.6:c.7634C= MANE Select	NP_071407.4:p.Thr2545=