Canonical Allele Identifier: CA470069185

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500584G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740827G>T , CM000672.2:g.71740827G>T	GRCh38
NC_000010.10:g.73500584G>T , CM000672.1:g.73500584G>T	GRCh37
NC_000010.9:g.73170590G>T	NCBI36
NG_008835.1:g.348881G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4494G>T MANE Select	ENSP00000224721.9:p.Val1498=
ENST00000224721.10:c.4509G>T	ENSP00000224721.8:p.Val1503=
ENST00000398792.3:n.1183G>T
ENST00000622827.4:c.4494G>T	ENSP00000483211.1:p.Val1498=
NM_022124.5:c.4494G>T	NP_071407.4:p.Val1498=
XM_006717940.2:c.4689G>T	XP_006718003.1:p.Val1563=
XM_006717942.2:c.4623G>T	XP_006718005.1:p.Val1541=
XM_011540039.1:c.4686G>T	XP_011538341.1:p.Val1562=
XM_011540040.1:c.4683G>T	XP_011538342.1:p.Val1561=
XM_011540041.1:c.4629G>T	XP_011538343.1:p.Val1543=
XM_011540042.1:c.4689G>T	XP_011538344.1:p.Val1563=
XM_011540043.1:c.4689G>T	XP_011538345.1:p.Val1563=
XM_011540044.1:c.4554G>T	XP_011538346.1:p.Val1518=
XM_011540045.1:c.4689G>T	XP_011538347.1:p.Val1563=
XM_011540046.1:c.4149G>T	XP_011538348.1:p.Val1383=
XM_011540047.1:c.3507G>T	XP_011538349.1:p.Val1169=
XM_011540048.1:c.4689G>T	XP_011538350.1:p.Val1563=
XM_011540049.1:c.4689G>T	XP_011538351.1:p.Val1563=
XM_011540050.1:c.4689G>T	XP_011538352.1:p.Val1563=
XM_011540051.1:c.4689G>T	XP_011538353.1:p.Val1563=
XM_011540052.1:c.1017G>T	XP_011538354.1:p.Val339=
XM_011540053.1:c.4689G>T	XP_011538355.1:p.Val1563=
XR_945796.1:n.4932G>T
NM_022124.6:c.4494G>T MANE Select	NP_071407.4:p.Val1498=