Canonical Allele Identifier: CA470282561

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567445C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807688C>G , CM000672.2:g.71807688C>G	GRCh38
NC_000010.10:g.73567445C>G , CM000672.1:g.73567445C>G	GRCh37
NC_000010.9:g.73237451C>G	NCBI36
NG_008835.1:g.415742C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8481C>G MANE Select	ENSP00000224721.9:p.Leu2827=
ENST00000642965.1:c.2414C>G	ENSP00000495222.1:n.2414C>G
ENST00000647092.1:c.2078C>G	ENSP00000495176.1:n.2078C>G
ENST00000224721.10:c.8496C>G	ENSP00000224721.8:p.Leu2832=
ENST00000398788.4:c.1761C>G	ENSP00000381768.3:p.Leu587=
ENST00000475158.1:n.2017C>G
ENST00000619887.4:c.1761C>G	ENSP00000478374.1:p.Leu587=
ENST00000622827.4:c.8481C>G	ENSP00000483211.1:p.Leu2827=
NM_001171933.1:c.1761C>G	NP_001165404.1:p.Leu587=
NM_001171934.1:c.1761C>G	NP_001165405.1:p.Leu587=
NM_022124.5:c.8481C>G	NP_071407.4:p.Leu2827=
XM_006717940.2:c.8676C>G	XP_006718003.1:p.Leu2892=
XM_006717942.2:c.8610C>G	XP_006718005.1:p.Leu2870=
XM_011540039.1:c.8673C>G	XP_011538341.1:p.Leu2891=
XM_011540040.1:c.8670C>G	XP_011538342.1:p.Leu2890=
XM_011540041.1:c.8616C>G	XP_011538343.1:p.Leu2872=
XM_011540042.1:c.8586C>G	XP_011538344.1:p.Leu2862=
XM_011540043.1:c.8676C>G	XP_011538345.1:p.Leu2892=
XM_011540044.1:c.8541C>G	XP_011538346.1:p.Leu2847=
XM_011540045.1:c.8676C>G	XP_011538347.1:p.Leu2892=
XM_011540046.1:c.8136C>G	XP_011538348.1:p.Leu2712=
XM_011540047.1:c.7494C>G	XP_011538349.1:p.Leu2498=
XM_011540052.1:c.5004C>G	XP_011538354.1:p.Leu1668=
NM_022124.6:c.8481C>G MANE Select	NP_071407.4:p.Leu2827=