Canonical Allele Identifier: CA470069260

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500695C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740938C>G , CM000672.2:g.71740938C>G	GRCh38
NC_000010.10:g.73500695C>G , CM000672.1:g.73500695C>G	GRCh37
NC_000010.9:g.73170701C>G	NCBI36
NG_008835.1:g.348992C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4605C>G MANE Select	ENSP00000224721.9:p.Val1535=
ENST00000224721.10:c.4620C>G	ENSP00000224721.8:p.Val1540=
ENST00000398792.3:n.1294C>G
ENST00000622827.4:c.4605C>G	ENSP00000483211.1:p.Val1535=
NM_022124.5:c.4605C>G	NP_071407.4:p.Val1535=
XM_006717940.2:c.4800C>G	XP_006718003.1:p.Val1600=
XM_006717942.2:c.4734C>G	XP_006718005.1:p.Val1578=
XM_011540039.1:c.4797C>G	XP_011538341.1:p.Val1599=
XM_011540040.1:c.4794C>G	XP_011538342.1:p.Val1598=
XM_011540041.1:c.4740C>G	XP_011538343.1:p.Val1580=
XM_011540042.1:c.4800C>G	XP_011538344.1:p.Val1600=
XM_011540043.1:c.4800C>G	XP_011538345.1:p.Val1600=
XM_011540044.1:c.4665C>G	XP_011538346.1:p.Val1555=
XM_011540045.1:c.4800C>G	XP_011538347.1:p.Val1600=
XM_011540046.1:c.4260C>G	XP_011538348.1:p.Val1420=
XM_011540047.1:c.3618C>G	XP_011538349.1:p.Val1206=
XM_011540048.1:c.4800C>G	XP_011538350.1:p.Val1600=
XM_011540049.1:c.4800C>G	XP_011538351.1:p.Val1600=
XM_011540050.1:c.4800C>G	XP_011538352.1:p.Val1600=
XM_011540051.1:c.4800C>G	XP_011538353.1:p.Val1600=
XM_011540052.1:c.1128C>G	XP_011538354.1:p.Val376=
XM_011540053.1:c.4800C>G	XP_011538355.1:p.Val1600=
XR_945796.1:n.5043C>G
NM_022124.6:c.4605C>G MANE Select	NP_071407.4:p.Val1535=