Canonical Allele Identifier: CA470060753

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544764C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785007C>T , CM000672.2:g.71785007C>T	GRCh38
NC_000010.10:g.73544764C>T , CM000672.1:g.73544764C>T	GRCh37
NC_000010.9:g.73214770C>T	NCBI36
NG_008835.1:g.393061C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5619C>T MANE Select	ENSP00000224721.9:p.Val1873=
ENST00000224721.10:c.5634C>T	ENSP00000224721.8:p.Val1878=
ENST00000622827.4:c.5619C>T	ENSP00000483211.1:p.Val1873=
NM_022124.5:c.5619C>T	NP_071407.4:p.Val1873=
XM_006717940.2:c.5814C>T	XP_006718003.1:p.Val1938=
XM_006717942.2:c.5748C>T	XP_006718005.1:p.Val1916=
XM_011540039.1:c.5811C>T	XP_011538341.1:p.Val1937=
XM_011540040.1:c.5808C>T	XP_011538342.1:p.Val1936=
XM_011540041.1:c.5754C>T	XP_011538343.1:p.Val1918=
XM_011540042.1:c.5814C>T	XP_011538344.1:p.Val1938=
XM_011540043.1:c.5814C>T	XP_011538345.1:p.Val1938=
XM_011540044.1:c.5679C>T	XP_011538346.1:p.Val1893=
XM_011540045.1:c.5814C>T	XP_011538347.1:p.Val1938=
XM_011540046.1:c.5274C>T	XP_011538348.1:p.Val1758=
XM_011540047.1:c.4632C>T	XP_011538349.1:p.Val1544=
XM_011540048.1:c.5814C>T	XP_011538350.1:p.Val1938=
XM_011540049.1:c.5814C>T	XP_011538351.1:p.Val1938=
XM_011540050.1:c.5814C>T	XP_011538352.1:p.Val1938=
XM_011540051.1:c.5814C>T	XP_011538353.1:p.Val1938=
XM_011540052.1:c.2142C>T	XP_011538354.1:p.Val714=
XM_011540053.1:c.5814C>T	XP_011538355.1:p.Val1938=
XR_945796.1:n.6057C>T
NM_022124.6:c.5619C>T MANE Select	NP_071407.4:p.Val1873=