Canonical Allele Identifier: CA1918853818

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740823T= , CM000672.2:g.71740823T=	GRCh38
NC_000010.10:g.73500580T= , CM000672.1:g.73500580T=	GRCh37
NC_000010.9:g.73170586T=	NCBI36
NG_008835.1:g.348877T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4490T= MANE Select	ENSP00000224721.9:p.Val1497=
ENST00000224721.10:c.4505T=	ENSP00000224721.8:p.Val1502=
ENST00000398792.3:n.1179T=
ENST00000622827.4:c.4490T=	ENSP00000483211.1:p.Val1497=
NM_022124.5:c.4490T=	NP_071407.4:p.Val1497=
XM_006717940.2:c.4685T=	XP_006718003.1:p.Val1562=
XM_006717942.2:c.4619T=	XP_006718005.1:p.Val1540=
XM_011540039.1:c.4682T=	XP_011538341.1:p.Val1561=
XM_011540040.1:c.4679T=	XP_011538342.1:p.Val1560=
XM_011540041.1:c.4625T=	XP_011538343.1:p.Val1542=
XM_011540042.1:c.4685T=	XP_011538344.1:p.Val1562=
XM_011540043.1:c.4685T=	XP_011538345.1:p.Val1562=
XM_011540044.1:c.4550T=	XP_011538346.1:p.Val1517=
XM_011540045.1:c.4685T=	XP_011538347.1:p.Val1562=
XM_011540046.1:c.4145T=	XP_011538348.1:p.Val1382=
XM_011540047.1:c.3503T=	XP_011538349.1:p.Val1168=
XM_011540048.1:c.4685T=	XP_011538350.1:p.Val1562=
XM_011540049.1:c.4685T=	XP_011538351.1:p.Val1562=
XM_011540050.1:c.4685T=	XP_011538352.1:p.Val1562=
XM_011540051.1:c.4685T=	XP_011538353.1:p.Val1562=
XM_011540052.1:c.1013T=	XP_011538354.1:p.Val338=
XM_011540053.1:c.4685T=	XP_011538355.1:p.Val1562=
XR_945796.1:n.4928T=
NM_022124.6:c.4490T= MANE Select	NP_071407.4:p.Val1497=