Canonical Allele Identifier: CA377147323

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544852G>A (hg19) ; chr10:g.71785095G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785095G>A , CM000672.2:g.71785095G>A	GRCh38
NC_000010.10:g.73544852G>A , CM000672.1:g.73544852G>A	GRCh37
NC_000010.9:g.73214858G>A	NCBI36
NG_008835.1:g.393149G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5707G>A MANE Select	ENSP00000224721.9:p.Ala1903Thr
ENST00000224721.10:c.5722G>A	ENSP00000224721.8:p.Ala1908Thr
ENST00000622827.4:c.5707G>A	ENSP00000483211.1:p.Ala1903Thr
NM_022124.5:c.5707G>A	NP_071407.4:p.Ala1903Thr
XM_006717940.2:c.5902G>A	XP_006718003.1:p.Ala1968Thr
XM_006717942.2:c.5836G>A	XP_006718005.1:p.Ala1946Thr
XM_011540039.1:c.5899G>A	XP_011538341.1:p.Ala1967Thr
XM_011540040.1:c.5896G>A	XP_011538342.1:p.Ala1966Thr
XM_011540041.1:c.5842G>A	XP_011538343.1:p.Ala1948Thr
XM_011540042.1:c.5902G>A	XP_011538344.1:p.Ala1968Thr
XM_011540043.1:c.5902G>A	XP_011538345.1:p.Ala1968Thr
XM_011540044.1:c.5767G>A	XP_011538346.1:p.Ala1923Thr
XM_011540045.1:c.5902G>A	XP_011538347.1:p.Ala1968Thr
XM_011540046.1:c.5362G>A	XP_011538348.1:p.Ala1788Thr
XM_011540047.1:c.4720G>A	XP_011538349.1:p.Ala1574Thr
XM_011540048.1:c.5902G>A	XP_011538350.1:p.Ala1968Thr
XM_011540049.1:c.5902G>A	XP_011538351.1:p.Ala1968Thr
XM_011540050.1:c.5902G>A	XP_011538352.1:p.Ala1968Thr
XM_011540051.1:c.5902G>A	XP_011538353.1:p.Ala1968Thr
XM_011540052.1:c.2230G>A	XP_011538354.1:p.Ala744Thr
XM_011540053.1:c.5902G>A	XP_011538355.1:p.Ala1968Thr
XR_945796.1:n.6145G>A
NM_022124.6:c.5707G>A MANE Select	NP_071407.4:p.Ala1903Thr