Canonical Allele Identifier: CA470069223

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500638C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740881C>A , CM000672.2:g.71740881C>A	GRCh38
NC_000010.10:g.73500638C>A , CM000672.1:g.73500638C>A	GRCh37
NC_000010.9:g.73170644C>A	NCBI36
NG_008835.1:g.348935C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4548C>A MANE Select	ENSP00000224721.9:p.Thr1516=
ENST00000224721.10:c.4563C>A	ENSP00000224721.8:p.Thr1521=
ENST00000398792.3:n.1237C>A
ENST00000622827.4:c.4548C>A	ENSP00000483211.1:p.Thr1516=
NM_022124.5:c.4548C>A	NP_071407.4:p.Thr1516=
XM_006717940.2:c.4743C>A	XP_006718003.1:p.Thr1581=
XM_006717942.2:c.4677C>A	XP_006718005.1:p.Thr1559=
XM_011540039.1:c.4740C>A	XP_011538341.1:p.Thr1580=
XM_011540040.1:c.4737C>A	XP_011538342.1:p.Thr1579=
XM_011540041.1:c.4683C>A	XP_011538343.1:p.Thr1561=
XM_011540042.1:c.4743C>A	XP_011538344.1:p.Thr1581=
XM_011540043.1:c.4743C>A	XP_011538345.1:p.Thr1581=
XM_011540044.1:c.4608C>A	XP_011538346.1:p.Thr1536=
XM_011540045.1:c.4743C>A	XP_011538347.1:p.Thr1581=
XM_011540046.1:c.4203C>A	XP_011538348.1:p.Thr1401=
XM_011540047.1:c.3561C>A	XP_011538349.1:p.Thr1187=
XM_011540048.1:c.4743C>A	XP_011538350.1:p.Thr1581=
XM_011540049.1:c.4743C>A	XP_011538351.1:p.Thr1581=
XM_011540050.1:c.4743C>A	XP_011538352.1:p.Thr1581=
XM_011540051.1:c.4743C>A	XP_011538353.1:p.Thr1581=
XM_011540052.1:c.1071C>A	XP_011538354.1:p.Thr357=
XM_011540053.1:c.4743C>A	XP_011538355.1:p.Thr1581=
XR_945796.1:n.4986C>A
NM_022124.6:c.4548C>A MANE Select	NP_071407.4:p.Thr1516=