Canonical Allele Identifier: CA470062080

Gene: CDH23

Linked Data

• gnomAD v4: 10-71798496-C-T
• MyVariant Identifiers: chr10:g.73558253C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798496C>T , CM000672.2:g.71798496C>T	GRCh38
NC_000010.10:g.73558253C>T , CM000672.1:g.73558253C>T	GRCh37
NC_000010.9:g.73228259C>T	NCBI36
NG_008835.1:g.406550C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6972C>T MANE Select	ENSP00000224721.9:p.Asp2324=
ENST00000642965.1:c.905C>T	ENSP00000495222.1:n.905C>T
ENST00000647092.1:c.569C>T	ENSP00000495176.1:n.569C>T
ENST00000224721.10:c.6987C>T	ENSP00000224721.8:p.Asp2329=
ENST00000398788.4:c.252C>T	ENSP00000381768.3:p.Asp84=
ENST00000475158.1:n.508C>T
ENST00000619887.4:c.252C>T	ENSP00000478374.1:p.Asp84=
ENST00000622827.4:c.6972C>T	ENSP00000483211.1:p.Asp2324=
NM_001171933.1:c.252C>T	NP_001165404.1:p.Asp84=
NM_001171934.1:c.252C>T	NP_001165405.1:p.Asp84=
NM_022124.5:c.6972C>T	NP_071407.4:p.Asp2324=
XM_006717940.2:c.7167C>T	XP_006718003.1:p.Asp2389=
XM_006717942.2:c.7101C>T	XP_006718005.1:p.Asp2367=
XM_011540039.1:c.7164C>T	XP_011538341.1:p.Asp2388=
XM_011540040.1:c.7161C>T	XP_011538342.1:p.Asp2387=
XM_011540041.1:c.7107C>T	XP_011538343.1:p.Asp2369=
XM_011540042.1:c.7077C>T	XP_011538344.1:p.Asp2359=
XM_011540043.1:c.7167C>T	XP_011538345.1:p.Asp2389=
XM_011540044.1:c.7032C>T	XP_011538346.1:p.Asp2344=
XM_011540045.1:c.7167C>T	XP_011538347.1:p.Asp2389=
XM_011540046.1:c.6627C>T	XP_011538348.1:p.Asp2209=
XM_011540047.1:c.5985C>T	XP_011538349.1:p.Asp1995=
XM_011540052.1:c.3495C>T	XP_011538354.1:p.Asp1165=
NM_022124.6:c.6972C>T MANE Select	NP_071407.4:p.Asp2324=