Canonical Allele Identifier: CA1918862363

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785017G= , CM000672.2:g.71785017G=	GRCh38
NC_000010.10:g.73544774G= , CM000672.1:g.73544774G=	GRCh37
NC_000010.9:g.73214780G=	NCBI36
NG_008835.1:g.393071G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5629G= MANE Select	ENSP00000224721.9:p.Asp1877=
ENST00000224721.10:c.5644G=	ENSP00000224721.8:p.Asp1882=
ENST00000622827.4:c.5629G=	ENSP00000483211.1:p.Asp1877=
NM_022124.5:c.5629G=	NP_071407.4:p.Asp1877=
XM_006717940.2:c.5824G=	XP_006718003.1:p.Asp1942=
XM_006717942.2:c.5758G=	XP_006718005.1:p.Asp1920=
XM_011540039.1:c.5821G=	XP_011538341.1:p.Asp1941=
XM_011540040.1:c.5818G=	XP_011538342.1:p.Asp1940=
XM_011540041.1:c.5764G=	XP_011538343.1:p.Asp1922=
XM_011540042.1:c.5824G=	XP_011538344.1:p.Asp1942=
XM_011540043.1:c.5824G=	XP_011538345.1:p.Asp1942=
XM_011540044.1:c.5689G=	XP_011538346.1:p.Asp1897=
XM_011540045.1:c.5824G=	XP_011538347.1:p.Asp1942=
XM_011540046.1:c.5284G=	XP_011538348.1:p.Asp1762=
XM_011540047.1:c.4642G=	XP_011538349.1:p.Asp1548=
XM_011540048.1:c.5824G=	XP_011538350.1:p.Asp1942=
XM_011540049.1:c.5824G=	XP_011538351.1:p.Asp1942=
XM_011540050.1:c.5824G=	XP_011538352.1:p.Asp1942=
XM_011540051.1:c.5824G=	XP_011538353.1:p.Asp1942=
XM_011540052.1:c.2152G=	XP_011538354.1:p.Asp718=
XM_011540053.1:c.5824G=	XP_011538355.1:p.Asp1942=
XR_945796.1:n.6067G=
NM_022124.6:c.5629G= MANE Select	NP_071407.4:p.Asp1877=