Canonical Allele Identifier: CA470282114

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559320C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799563C>A , CM000672.2:g.71799563C>A	GRCh38
NC_000010.10:g.73559320C>A , CM000672.1:g.73559320C>A	GRCh37
NC_000010.9:g.73229326C>A	NCBI36
NG_008835.1:g.407617C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7296C>A MANE Select	ENSP00000224721.9:p.Gly2432=
ENST00000642965.1:c.1229C>A	ENSP00000495222.1:n.1229C>A
ENST00000647092.1:c.893C>A	ENSP00000495176.1:n.893C>A
ENST00000224721.10:c.7311C>A	ENSP00000224721.8:p.Gly2437=
ENST00000398788.4:c.576C>A	ENSP00000381768.3:p.Gly192=
ENST00000475158.1:n.832C>A
ENST00000619887.4:c.576C>A	ENSP00000478374.1:p.Gly192=
ENST00000622827.4:c.7296C>A	ENSP00000483211.1:p.Gly2432=
NM_001171933.1:c.576C>A	NP_001165404.1:p.Gly192=
NM_001171934.1:c.576C>A	NP_001165405.1:p.Gly192=
NM_022124.5:c.7296C>A	NP_071407.4:p.Gly2432=
XM_006717940.2:c.7491C>A	XP_006718003.1:p.Gly2497=
XM_006717942.2:c.7425C>A	XP_006718005.1:p.Gly2475=
XM_011540039.1:c.7488C>A	XP_011538341.1:p.Gly2496=
XM_011540040.1:c.7485C>A	XP_011538342.1:p.Gly2495=
XM_011540041.1:c.7431C>A	XP_011538343.1:p.Gly2477=
XM_011540042.1:c.7401C>A	XP_011538344.1:p.Gly2467=
XM_011540043.1:c.7491C>A	XP_011538345.1:p.Gly2497=
XM_011540044.1:c.7356C>A	XP_011538346.1:p.Gly2452=
XM_011540045.1:c.7491C>A	XP_011538347.1:p.Gly2497=
XM_011540046.1:c.6951C>A	XP_011538348.1:p.Gly2317=
XM_011540047.1:c.6309C>A	XP_011538349.1:p.Gly2103=
XM_011540052.1:c.3819C>A	XP_011538354.1:p.Gly1273=
NM_022124.6:c.7296C>A MANE Select	NP_071407.4:p.Gly2432=