Canonical Allele Identifier: CA377160361

Gene: CDH23

Linked Data

• gnomAD v4: 10-71740841-G-T
• MyVariant Identifiers: chr10:g.73500598G>T (hg19) ; chr10:g.71740841G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740841G>T , CM000672.2:g.71740841G>T	GRCh38
NC_000010.10:g.73500598G>T , CM000672.1:g.73500598G>T	GRCh37
NC_000010.9:g.73170604G>T	NCBI36
NG_008835.1:g.348895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4508G>T MANE Select	ENSP00000224721.9:p.Gly1503Val
ENST00000224721.10:c.4523G>T	ENSP00000224721.8:p.Gly1508Val
ENST00000398792.3:n.1197G>T
ENST00000622827.4:c.4508G>T	ENSP00000483211.1:p.Gly1503Val
NM_022124.5:c.4508G>T	NP_071407.4:p.Gly1503Val
XM_006717940.2:c.4703G>T	XP_006718003.1:p.Gly1568Val
XM_006717942.2:c.4637G>T	XP_006718005.1:p.Gly1546Val
XM_011540039.1:c.4700G>T	XP_011538341.1:p.Gly1567Val
XM_011540040.1:c.4697G>T	XP_011538342.1:p.Gly1566Val
XM_011540041.1:c.4643G>T	XP_011538343.1:p.Gly1548Val
XM_011540042.1:c.4703G>T	XP_011538344.1:p.Gly1568Val
XM_011540043.1:c.4703G>T	XP_011538345.1:p.Gly1568Val
XM_011540044.1:c.4568G>T	XP_011538346.1:p.Gly1523Val
XM_011540045.1:c.4703G>T	XP_011538347.1:p.Gly1568Val
XM_011540046.1:c.4163G>T	XP_011538348.1:p.Gly1388Val
XM_011540047.1:c.3521G>T	XP_011538349.1:p.Gly1174Val
XM_011540048.1:c.4703G>T	XP_011538350.1:p.Gly1568Val
XM_011540049.1:c.4703G>T	XP_011538351.1:p.Gly1568Val
XM_011540050.1:c.4703G>T	XP_011538352.1:p.Gly1568Val
XM_011540051.1:c.4703G>T	XP_011538353.1:p.Gly1568Val
XM_011540052.1:c.1031G>T	XP_011538354.1:p.Gly344Val
XM_011540053.1:c.4703G>T	XP_011538355.1:p.Gly1568Val
XR_945796.1:n.4946G>T
NM_022124.6:c.4508G>T MANE Select	NP_071407.4:p.Gly1503Val