Canonical Allele Identifier: CA377160824

Gene: CDH23

Linked Data

• COSMIC: COSM5823659 ; COSM5823660
• MyVariant Identifiers: chr10:g.73500706A>T (hg19) ; chr10:g.71740949A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740949A>T , CM000672.2:g.71740949A>T	GRCh38
NC_000010.10:g.73500706A>T , CM000672.1:g.73500706A>T	GRCh37
NC_000010.9:g.73170712A>T	NCBI36
NG_008835.1:g.349003A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4616A>T MANE Select	ENSP00000224721.9:p.Glu1539Val
ENST00000224721.10:c.4631A>T	ENSP00000224721.8:p.Glu1544Val
ENST00000398792.3:n.1305A>T
ENST00000622827.4:c.4616A>T	ENSP00000483211.1:p.Glu1539Val
NM_022124.5:c.4616A>T	NP_071407.4:p.Glu1539Val
XM_006717940.2:c.4811A>T	XP_006718003.1:p.Glu1604Val
XM_006717942.2:c.4745A>T	XP_006718005.1:p.Glu1582Val
XM_011540039.1:c.4808A>T	XP_011538341.1:p.Glu1603Val
XM_011540040.1:c.4805A>T	XP_011538342.1:p.Glu1602Val
XM_011540041.1:c.4751A>T	XP_011538343.1:p.Glu1584Val
XM_011540042.1:c.4811A>T	XP_011538344.1:p.Glu1604Val
XM_011540043.1:c.4811A>T	XP_011538345.1:p.Glu1604Val
XM_011540044.1:c.4676A>T	XP_011538346.1:p.Glu1559Val
XM_011540045.1:c.4811A>T	XP_011538347.1:p.Glu1604Val
XM_011540046.1:c.4271A>T	XP_011538348.1:p.Glu1424Val
XM_011540047.1:c.3629A>T	XP_011538349.1:p.Glu1210Val
XM_011540048.1:c.4811A>T	XP_011538350.1:p.Glu1604Val
XM_011540049.1:c.4811A>T	XP_011538351.1:p.Glu1604Val
XM_011540050.1:c.4811A>T	XP_011538352.1:p.Glu1604Val
XM_011540051.1:c.4811A>T	XP_011538353.1:p.Glu1604Val
XM_011540052.1:c.1139A>T	XP_011538354.1:p.Glu380Val
XM_011540053.1:c.4811A>T	XP_011538355.1:p.Glu1604Val
XR_945796.1:n.5054A>T
NM_022124.6:c.4616A>T MANE Select	NP_071407.4:p.Glu1539Val