Canonical Allele Identifier: CA377160566

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500648A>G (hg19) ; chr10:g.71740891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740891A>G , CM000672.2:g.71740891A>G	GRCh38
NC_000010.10:g.73500648A>G , CM000672.1:g.73500648A>G	GRCh37
NC_000010.9:g.73170654A>G	NCBI36
NG_008835.1:g.348945A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4558A>G MANE Select	ENSP00000224721.9:p.Ile1520Val
ENST00000224721.10:c.4573A>G	ENSP00000224721.8:p.Ile1525Val
ENST00000398792.3:n.1247A>G
ENST00000622827.4:c.4558A>G	ENSP00000483211.1:p.Ile1520Val
NM_022124.5:c.4558A>G	NP_071407.4:p.Ile1520Val
XM_006717940.2:c.4753A>G	XP_006718003.1:p.Ile1585Val
XM_006717942.2:c.4687A>G	XP_006718005.1:p.Ile1563Val
XM_011540039.1:c.4750A>G	XP_011538341.1:p.Ile1584Val
XM_011540040.1:c.4747A>G	XP_011538342.1:p.Ile1583Val
XM_011540041.1:c.4693A>G	XP_011538343.1:p.Ile1565Val
XM_011540042.1:c.4753A>G	XP_011538344.1:p.Ile1585Val
XM_011540043.1:c.4753A>G	XP_011538345.1:p.Ile1585Val
XM_011540044.1:c.4618A>G	XP_011538346.1:p.Ile1540Val
XM_011540045.1:c.4753A>G	XP_011538347.1:p.Ile1585Val
XM_011540046.1:c.4213A>G	XP_011538348.1:p.Ile1405Val
XM_011540047.1:c.3571A>G	XP_011538349.1:p.Ile1191Val
XM_011540048.1:c.4753A>G	XP_011538350.1:p.Ile1585Val
XM_011540049.1:c.4753A>G	XP_011538351.1:p.Ile1585Val
XM_011540050.1:c.4753A>G	XP_011538352.1:p.Ile1585Val
XM_011540051.1:c.4753A>G	XP_011538353.1:p.Ile1585Val
XM_011540052.1:c.1081A>G	XP_011538354.1:p.Ile361Val
XM_011540053.1:c.4753A>G	XP_011538355.1:p.Ile1585Val
XR_945796.1:n.4996A>G
NM_022124.6:c.4558A>G MANE Select	NP_071407.4:p.Ile1520Val