Canonical Allele Identifier: CA377158100

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558253C>A (hg19) ; chr10:g.71798496C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6972C>A MANE Select	ENSP00000224721.9:p.Asp2324Glu
ENST00000642965.1:c.905C>A	ENSP00000495222.1:n.905C>A
ENST00000647092.1:c.569C>A	ENSP00000495176.1:n.569C>A
ENST00000224721.10:c.6987C>A	ENSP00000224721.8:p.Asp2329Glu
ENST00000398788.4:c.252C>A	ENSP00000381768.3:p.Asp84Glu
ENST00000475158.1:n.508C>A
ENST00000619887.4:c.252C>A	ENSP00000478374.1:p.Asp84Glu
ENST00000622827.4:c.6972C>A	ENSP00000483211.1:p.Asp2324Glu
NM_001171933.1:c.252C>A	NP_001165404.1:p.Asp84Glu
NM_001171934.1:c.252C>A	NP_001165405.1:p.Asp84Glu
NM_022124.5:c.6972C>A	NP_071407.4:p.Asp2324Glu
XM_006717940.2:c.7167C>A	XP_006718003.1:p.Asp2389Glu
XM_006717942.2:c.7101C>A	XP_006718005.1:p.Asp2367Glu
XM_011540039.1:c.7164C>A	XP_011538341.1:p.Asp2388Glu
XM_011540040.1:c.7161C>A	XP_011538342.1:p.Asp2387Glu
XM_011540041.1:c.7107C>A	XP_011538343.1:p.Asp2369Glu
XM_011540042.1:c.7077C>A	XP_011538344.1:p.Asp2359Glu
XM_011540043.1:c.7167C>A	XP_011538345.1:p.Asp2389Glu
XM_011540044.1:c.7032C>A	XP_011538346.1:p.Asp2344Glu
XM_011540045.1:c.7167C>A	XP_011538347.1:p.Asp2389Glu
XM_011540046.1:c.6627C>A	XP_011538348.1:p.Asp2209Glu
XM_011540047.1:c.5985C>A	XP_011538349.1:p.Asp1995Glu
XM_011540052.1:c.3495C>A	XP_011538354.1:p.Asp1165Glu
NM_022124.6:c.6972C>A MANE Select	NP_071407.4:p.Asp2324Glu