Canonical Allele Identifier: CA470060709

Gene: CDH23

Linked Data

• gnomAD v4: 10-71784938-G-T
• MyVariant Identifiers: chr10:g.73544695G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784938G>T , CM000672.2:g.71784938G>T	GRCh38
NC_000010.10:g.73544695G>T , CM000672.1:g.73544695G>T	GRCh37
NC_000010.9:g.73214701G>T	NCBI36
NG_008835.1:g.392992G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5550G>T MANE Select	ENSP00000224721.9:p.Val1850=
ENST00000224721.10:c.5565G>T	ENSP00000224721.8:p.Val1855=
ENST00000622827.4:c.5550G>T	ENSP00000483211.1:p.Val1850=
NM_022124.5:c.5550G>T	NP_071407.4:p.Val1850=
XM_006717940.2:c.5745G>T	XP_006718003.1:p.Val1915=
XM_006717942.2:c.5679G>T	XP_006718005.1:p.Val1893=
XM_011540039.1:c.5742G>T	XP_011538341.1:p.Val1914=
XM_011540040.1:c.5739G>T	XP_011538342.1:p.Val1913=
XM_011540041.1:c.5685G>T	XP_011538343.1:p.Val1895=
XM_011540042.1:c.5745G>T	XP_011538344.1:p.Val1915=
XM_011540043.1:c.5745G>T	XP_011538345.1:p.Val1915=
XM_011540044.1:c.5610G>T	XP_011538346.1:p.Val1870=
XM_011540045.1:c.5745G>T	XP_011538347.1:p.Val1915=
XM_011540046.1:c.5205G>T	XP_011538348.1:p.Val1735=
XM_011540047.1:c.4563G>T	XP_011538349.1:p.Val1521=
XM_011540048.1:c.5745G>T	XP_011538350.1:p.Val1915=
XM_011540049.1:c.5745G>T	XP_011538351.1:p.Val1915=
XM_011540050.1:c.5745G>T	XP_011538352.1:p.Val1915=
XM_011540051.1:c.5745G>T	XP_011538353.1:p.Val1915=
XM_011540052.1:c.2073G>T	XP_011538354.1:p.Val691=
XM_011540053.1:c.5745G>T	XP_011538355.1:p.Val1915=
XR_945796.1:n.5988G>T
NM_022124.6:c.5550G>T MANE Select	NP_071407.4:p.Val1850=