Canonical Allele Identifier: CA377146249

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544655T>G (hg19) ; chr10:g.71784898T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784898T>G , CM000672.2:g.71784898T>G	GRCh38
NC_000010.10:g.73544655T>G , CM000672.1:g.73544655T>G	GRCh37
NC_000010.9:g.73214661T>G	NCBI36
NG_008835.1:g.392952T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5510T>G MANE Select	ENSP00000224721.9:p.Val1837Gly
ENST00000224721.10:c.5525T>G	ENSP00000224721.8:p.Val1842Gly
ENST00000622827.4:c.5510T>G	ENSP00000483211.1:p.Val1837Gly
NM_022124.5:c.5510T>G	NP_071407.4:p.Val1837Gly
XM_006717940.2:c.5705T>G	XP_006718003.1:p.Val1902Gly
XM_006717942.2:c.5639T>G	XP_006718005.1:p.Val1880Gly
XM_011540039.1:c.5702T>G	XP_011538341.1:p.Val1901Gly
XM_011540040.1:c.5699T>G	XP_011538342.1:p.Val1900Gly
XM_011540041.1:c.5645T>G	XP_011538343.1:p.Val1882Gly
XM_011540042.1:c.5705T>G	XP_011538344.1:p.Val1902Gly
XM_011540043.1:c.5705T>G	XP_011538345.1:p.Val1902Gly
XM_011540044.1:c.5570T>G	XP_011538346.1:p.Val1857Gly
XM_011540045.1:c.5705T>G	XP_011538347.1:p.Val1902Gly
XM_011540046.1:c.5165T>G	XP_011538348.1:p.Val1722Gly
XM_011540047.1:c.4523T>G	XP_011538349.1:p.Val1508Gly
XM_011540048.1:c.5705T>G	XP_011538350.1:p.Val1902Gly
XM_011540049.1:c.5705T>G	XP_011538351.1:p.Val1902Gly
XM_011540050.1:c.5705T>G	XP_011538352.1:p.Val1902Gly
XM_011540051.1:c.5705T>G	XP_011538353.1:p.Val1902Gly
XM_011540052.1:c.2033T>G	XP_011538354.1:p.Val678Gly
XM_011540053.1:c.5705T>G	XP_011538355.1:p.Val1902Gly
XR_945796.1:n.5948T>G
NM_022124.6:c.5510T>G MANE Select	NP_071407.4:p.Val1837Gly