Canonical Allele Identifier: CA470282442

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567358C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807601C>A , CM000672.2:g.71807601C>A	GRCh38
NC_000010.10:g.73567358C>A , CM000672.1:g.73567358C>A	GRCh37
NC_000010.9:g.73237364C>A	NCBI36
NG_008835.1:g.415655C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8394C>A MANE Select	ENSP00000224721.9:p.Ile2798=
ENST00000642965.1:c.2327C>A	ENSP00000495222.1:n.2327C>A
ENST00000647092.1:c.1991C>A	ENSP00000495176.1:n.1991C>A
ENST00000224721.10:c.8409C>A	ENSP00000224721.8:p.Ile2803=
ENST00000398788.4:c.1674C>A	ENSP00000381768.3:p.Ile558=
ENST00000475158.1:n.1930C>A
ENST00000619887.4:c.1674C>A	ENSP00000478374.1:p.Ile558=
ENST00000622827.4:c.8394C>A	ENSP00000483211.1:p.Ile2798=
NM_001171933.1:c.1674C>A	NP_001165404.1:p.Ile558=
NM_001171934.1:c.1674C>A	NP_001165405.1:p.Ile558=
NM_022124.5:c.8394C>A	NP_071407.4:p.Ile2798=
XM_006717940.2:c.8589C>A	XP_006718003.1:p.Ile2863=
XM_006717942.2:c.8523C>A	XP_006718005.1:p.Ile2841=
XM_011540039.1:c.8586C>A	XP_011538341.1:p.Ile2862=
XM_011540040.1:c.8583C>A	XP_011538342.1:p.Ile2861=
XM_011540041.1:c.8529C>A	XP_011538343.1:p.Ile2843=
XM_011540042.1:c.8499C>A	XP_011538344.1:p.Ile2833=
XM_011540043.1:c.8589C>A	XP_011538345.1:p.Ile2863=
XM_011540044.1:c.8454C>A	XP_011538346.1:p.Ile2818=
XM_011540045.1:c.8589C>A	XP_011538347.1:p.Ile2863=
XM_011540046.1:c.8049C>A	XP_011538348.1:p.Ile2683=
XM_011540047.1:c.7407C>A	XP_011538349.1:p.Ile2469=
XM_011540052.1:c.4917C>A	XP_011538354.1:p.Ile1639=
NM_022124.6:c.8394C>A MANE Select	NP_071407.4:p.Ile2798=