Canonical Allele Identifier: CA1918874631

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793542C= , CM000672.2:g.71793542C=	GRCh38
NC_000010.10:g.73553299C= , CM000672.1:g.73553299C=	GRCh37
NC_000010.9:g.73223305C=	NCBI36
NG_008835.1:g.401596C=

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.6614C= MANE Select	NP_071407.4:p.Pro2205=
ENST00000224721.12:c.6614C= MANE Select	ENSP00000224721.9:p.Pro2205=
NM_022124.5:c.6614C=	NP_071407.4:p.Pro2205=
ENST00000224721.10:c.6629C=	ENSP00000224721.8:p.Pro2210=
ENST00000622827.4:c.6614C=	ENSP00000483211.1:p.Pro2205=
XM_006717940.2:c.6809C=	XP_006718003.1:p.Pro2270=
XM_006717942.2:c.6743C=	XP_006718005.1:p.Pro2248=
XM_011540039.1:c.6806C=	XP_011538341.1:p.Pro2269=
XM_011540040.1:c.6803C=	XP_011538342.1:p.Pro2268=
XM_011540041.1:c.6749C=	XP_011538343.1:p.Pro2250=
XM_011540042.1:c.6719C=	XP_011538344.1:p.Pro2240=
XM_011540043.1:c.6809C=	XP_011538345.1:p.Pro2270=
XM_011540044.1:c.6674C=	XP_011538346.1:p.Pro2225=
XM_011540045.1:c.6809C=	XP_011538347.1:p.Pro2270=
XM_011540046.1:c.6269C=	XP_011538348.1:p.Pro2090=
XM_011540047.1:c.5627C=	XP_011538349.1:p.Pro1876=
XM_011540048.1:c.6809C=	XP_011538350.1:p.Pro2270=
XM_011540049.1:c.6809C=	XP_011538351.1:p.Pro2270=
XM_011540050.1:c.6809C=	XP_011538352.1:p.Pro2270=
XM_011540051.1:c.6809C=	XP_011538353.1:p.Pro2270=
XM_011540052.1:c.3137C=	XP_011538354.1:p.Pro1046=
XR_945796.1:n.7052C=