Canonical Allele Identifier: CA470069189

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500590T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740833T>A , CM000672.2:g.71740833T>A	GRCh38
NC_000010.10:g.73500590T>A , CM000672.1:g.73500590T>A	GRCh37
NC_000010.9:g.73170596T>A	NCBI36
NG_008835.1:g.348887T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4500T>A MANE Select	ENSP00000224721.9:p.Ser1500=
ENST00000224721.10:c.4515T>A	ENSP00000224721.8:p.Ser1505=
ENST00000398792.3:n.1189T>A
ENST00000622827.4:c.4500T>A	ENSP00000483211.1:p.Ser1500=
NM_022124.5:c.4500T>A	NP_071407.4:p.Ser1500=
XM_006717940.2:c.4695T>A	XP_006718003.1:p.Ser1565=
XM_006717942.2:c.4629T>A	XP_006718005.1:p.Ser1543=
XM_011540039.1:c.4692T>A	XP_011538341.1:p.Ser1564=
XM_011540040.1:c.4689T>A	XP_011538342.1:p.Ser1563=
XM_011540041.1:c.4635T>A	XP_011538343.1:p.Ser1545=
XM_011540042.1:c.4695T>A	XP_011538344.1:p.Ser1565=
XM_011540043.1:c.4695T>A	XP_011538345.1:p.Ser1565=
XM_011540044.1:c.4560T>A	XP_011538346.1:p.Ser1520=
XM_011540045.1:c.4695T>A	XP_011538347.1:p.Ser1565=
XM_011540046.1:c.4155T>A	XP_011538348.1:p.Ser1385=
XM_011540047.1:c.3513T>A	XP_011538349.1:p.Ser1171=
XM_011540048.1:c.4695T>A	XP_011538350.1:p.Ser1565=
XM_011540049.1:c.4695T>A	XP_011538351.1:p.Ser1565=
XM_011540050.1:c.4695T>A	XP_011538352.1:p.Ser1565=
XM_011540051.1:c.4695T>A	XP_011538353.1:p.Ser1565=
XM_011540052.1:c.1023T>A	XP_011538354.1:p.Ser341=
XM_011540053.1:c.4695T>A	XP_011538355.1:p.Ser1565=
XR_945796.1:n.4938T>A
NM_022124.6:c.4500T>A MANE Select	NP_071407.4:p.Ser1500=