Canonical Allele Identifier: CA470282103

Gene: CDH23

Linked Data

• dbSNP Id: rs1256141143
• gnomAD v2: 10-73559311-T-G
• gnomAD v4: 10-71799554-T-G
• MyVariant Identifiers: chr10:g.73559311T>G (hg19) ; chr10:g.71799554T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799554T>G , CM000672.2:g.71799554T>G	GRCh38
NC_000010.10:g.73559311T>G , CM000672.1:g.73559311T>G	GRCh37
NC_000010.9:g.73229317T>G	NCBI36
NG_008835.1:g.407608T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7287T>G MANE Select	ENSP00000224721.9:p.Ala2429=
ENST00000642965.1:c.1220T>G	ENSP00000495222.1:n.1220T>G
ENST00000647092.1:c.884T>G	ENSP00000495176.1:n.884T>G
ENST00000224721.10:c.7302T>G	ENSP00000224721.8:p.Ala2434=
ENST00000398788.4:c.567T>G	ENSP00000381768.3:p.Ala189=
ENST00000475158.1:n.823T>G
ENST00000619887.4:c.567T>G	ENSP00000478374.1:p.Ala189=
ENST00000622827.4:c.7287T>G	ENSP00000483211.1:p.Ala2429=
NM_001171933.1:c.567T>G	NP_001165404.1:p.Ala189=
NM_001171934.1:c.567T>G	NP_001165405.1:p.Ala189=
NM_022124.5:c.7287T>G	NP_071407.4:p.Ala2429=
XM_006717940.2:c.7482T>G	XP_006718003.1:p.Ala2494=
XM_006717942.2:c.7416T>G	XP_006718005.1:p.Ala2472=
XM_011540039.1:c.7479T>G	XP_011538341.1:p.Ala2493=
XM_011540040.1:c.7476T>G	XP_011538342.1:p.Ala2492=
XM_011540041.1:c.7422T>G	XP_011538343.1:p.Ala2474=
XM_011540042.1:c.7392T>G	XP_011538344.1:p.Ala2464=
XM_011540043.1:c.7482T>G	XP_011538345.1:p.Ala2494=
XM_011540044.1:c.7347T>G	XP_011538346.1:p.Ala2449=
XM_011540045.1:c.7482T>G	XP_011538347.1:p.Ala2494=
XM_011540046.1:c.6942T>G	XP_011538348.1:p.Ala2314=
XM_011540047.1:c.6300T>G	XP_011538349.1:p.Ala2100=
XM_011540052.1:c.3810T>G	XP_011538354.1:p.Ala1270=
NM_022124.6:c.7287T>G MANE Select	NP_071407.4:p.Ala2429=