Canonical Allele Identifier: CA470282616

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567475G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807718G>A , CM000672.2:g.71807718G>A	GRCh38
NC_000010.10:g.73567475G>A , CM000672.1:g.73567475G>A	GRCh37
NC_000010.9:g.73237481G>A	NCBI36
NG_008835.1:g.415772G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8511G>A MANE Select	ENSP00000224721.9:p.Glu2837=
ENST00000642965.1:c.2444G>A	ENSP00000495222.1:n.2444G>A
ENST00000647092.1:c.2108G>A	ENSP00000495176.1:n.2108G>A
ENST00000224721.10:c.8526G>A	ENSP00000224721.8:p.Glu2842=
ENST00000398788.4:c.1791G>A	ENSP00000381768.3:p.Glu597=
ENST00000475158.1:n.2047G>A
ENST00000619887.4:c.1791G>A	ENSP00000478374.1:p.Glu597=
ENST00000622827.4:c.8511G>A	ENSP00000483211.1:p.Glu2837=
NM_001171933.1:c.1791G>A	NP_001165404.1:p.Glu597=
NM_001171934.1:c.1791G>A	NP_001165405.1:p.Glu597=
NM_022124.5:c.8511G>A	NP_071407.4:p.Glu2837=
XM_006717940.2:c.8706G>A	XP_006718003.1:p.Glu2902=
XM_006717942.2:c.8640G>A	XP_006718005.1:p.Glu2880=
XM_011540039.1:c.8703G>A	XP_011538341.1:p.Glu2901=
XM_011540040.1:c.8700G>A	XP_011538342.1:p.Glu2900=
XM_011540041.1:c.8646G>A	XP_011538343.1:p.Glu2882=
XM_011540042.1:c.8616G>A	XP_011538344.1:p.Glu2872=
XM_011540043.1:c.8706G>A	XP_011538345.1:p.Glu2902=
XM_011540044.1:c.8571G>A	XP_011538346.1:p.Glu2857=
XM_011540045.1:c.8706G>A	XP_011538347.1:p.Glu2902=
XM_011540046.1:c.8166G>A	XP_011538348.1:p.Glu2722=
XM_011540047.1:c.7524G>A	XP_011538349.1:p.Glu2508=
XM_011540052.1:c.5034G>A	XP_011538354.1:p.Glu1678=
NM_022124.6:c.8511G>A MANE Select	NP_071407.4:p.Glu2837=