Canonical Allele Identifier: CA377160768

Gene: CDH23

Linked Data

• gnomAD v4: 10-71740936-G-A
• MyVariant Identifiers: chr10:g.73500693G>A (hg19) ; chr10:g.71740936G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740936G>A , CM000672.2:g.71740936G>A	GRCh38
NC_000010.10:g.73500693G>A , CM000672.1:g.73500693G>A	GRCh37
NC_000010.9:g.73170699G>A	NCBI36
NG_008835.1:g.348990G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4603G>A MANE Select	ENSP00000224721.9:p.Val1535Ile
ENST00000224721.10:c.4618G>A	ENSP00000224721.8:p.Val1540Ile
ENST00000398792.3:n.1292G>A
ENST00000622827.4:c.4603G>A	ENSP00000483211.1:p.Val1535Ile
NM_022124.5:c.4603G>A	NP_071407.4:p.Val1535Ile
XM_006717940.2:c.4798G>A	XP_006718003.1:p.Val1600Ile
XM_006717942.2:c.4732G>A	XP_006718005.1:p.Val1578Ile
XM_011540039.1:c.4795G>A	XP_011538341.1:p.Val1599Ile
XM_011540040.1:c.4792G>A	XP_011538342.1:p.Val1598Ile
XM_011540041.1:c.4738G>A	XP_011538343.1:p.Val1580Ile
XM_011540042.1:c.4798G>A	XP_011538344.1:p.Val1600Ile
XM_011540043.1:c.4798G>A	XP_011538345.1:p.Val1600Ile
XM_011540044.1:c.4663G>A	XP_011538346.1:p.Val1555Ile
XM_011540045.1:c.4798G>A	XP_011538347.1:p.Val1600Ile
XM_011540046.1:c.4258G>A	XP_011538348.1:p.Val1420Ile
XM_011540047.1:c.3616G>A	XP_011538349.1:p.Val1206Ile
XM_011540048.1:c.4798G>A	XP_011538350.1:p.Val1600Ile
XM_011540049.1:c.4798G>A	XP_011538351.1:p.Val1600Ile
XM_011540050.1:c.4798G>A	XP_011538352.1:p.Val1600Ile
XM_011540051.1:c.4798G>A	XP_011538353.1:p.Val1600Ile
XM_011540052.1:c.1126G>A	XP_011538354.1:p.Val376Ile
XM_011540053.1:c.4798G>A	XP_011538355.1:p.Val1600Ile
XR_945796.1:n.5041G>A
NM_022124.6:c.4603G>A MANE Select	NP_071407.4:p.Val1535Ile