Canonical Allele Identifier: CA1918862077

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784910T= , CM000672.2:g.71784910T=	GRCh38
NC_000010.10:g.73544667T= , CM000672.1:g.73544667T=	GRCh37
NC_000010.9:g.73214673T=	NCBI36
NG_008835.1:g.392964T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5522T= MANE Select	ENSP00000224721.9:p.Val1841=
ENST00000224721.10:c.5537T=	ENSP00000224721.8:p.Val1846=
ENST00000622827.4:c.5522T=	ENSP00000483211.1:p.Val1841=
NM_022124.5:c.5522T=	NP_071407.4:p.Val1841=
XM_006717940.2:c.5717T=	XP_006718003.1:p.Val1906=
XM_006717942.2:c.5651T=	XP_006718005.1:p.Val1884=
XM_011540039.1:c.5714T=	XP_011538341.1:p.Val1905=
XM_011540040.1:c.5711T=	XP_011538342.1:p.Val1904=
XM_011540041.1:c.5657T=	XP_011538343.1:p.Val1886=
XM_011540042.1:c.5717T=	XP_011538344.1:p.Val1906=
XM_011540043.1:c.5717T=	XP_011538345.1:p.Val1906=
XM_011540044.1:c.5582T=	XP_011538346.1:p.Val1861=
XM_011540045.1:c.5717T=	XP_011538347.1:p.Val1906=
XM_011540046.1:c.5177T=	XP_011538348.1:p.Val1726=
XM_011540047.1:c.4535T=	XP_011538349.1:p.Val1512=
XM_011540048.1:c.5717T=	XP_011538350.1:p.Val1906=
XM_011540049.1:c.5717T=	XP_011538351.1:p.Val1906=
XM_011540050.1:c.5717T=	XP_011538352.1:p.Val1906=
XM_011540051.1:c.5717T=	XP_011538353.1:p.Val1906=
XM_011540052.1:c.2045T=	XP_011538354.1:p.Val682=
XM_011540053.1:c.5717T=	XP_011538355.1:p.Val1906=
XR_945796.1:n.5960T=
NM_022124.6:c.5522T= MANE Select	NP_071407.4:p.Val1841=