Canonical Allele Identifier: CA470062182

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558313C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798556C>T , CM000672.2:g.71798556C>T	GRCh38
NC_000010.10:g.73558313C>T , CM000672.1:g.73558313C>T	GRCh37
NC_000010.9:g.73228319C>T	NCBI36
NG_008835.1:g.406610C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7032C>T MANE Select	ENSP00000224721.9:p.Val2344=
ENST00000642965.1:c.965C>T	ENSP00000495222.1:n.965C>T
ENST00000647092.1:c.629C>T	ENSP00000495176.1:n.629C>T
ENST00000224721.10:c.7047C>T	ENSP00000224721.8:p.Val2349=
ENST00000398788.4:c.312C>T	ENSP00000381768.3:p.Val104=
ENST00000475158.1:n.568C>T
ENST00000619887.4:c.312C>T	ENSP00000478374.1:p.Val104=
ENST00000622827.4:c.7032C>T	ENSP00000483211.1:p.Val2344=
NM_001171933.1:c.312C>T	NP_001165404.1:p.Val104=
NM_001171934.1:c.312C>T	NP_001165405.1:p.Val104=
NM_022124.5:c.7032C>T	NP_071407.4:p.Val2344=
XM_006717940.2:c.7227C>T	XP_006718003.1:p.Val2409=
XM_006717942.2:c.7161C>T	XP_006718005.1:p.Val2387=
XM_011540039.1:c.7224C>T	XP_011538341.1:p.Val2408=
XM_011540040.1:c.7221C>T	XP_011538342.1:p.Val2407=
XM_011540041.1:c.7167C>T	XP_011538343.1:p.Val2389=
XM_011540042.1:c.7137C>T	XP_011538344.1:p.Val2379=
XM_011540043.1:c.7227C>T	XP_011538345.1:p.Val2409=
XM_011540044.1:c.7092C>T	XP_011538346.1:p.Val2364=
XM_011540045.1:c.7227C>T	XP_011538347.1:p.Val2409=
XM_011540046.1:c.6687C>T	XP_011538348.1:p.Val2229=
XM_011540047.1:c.6045C>T	XP_011538349.1:p.Val2015=
XM_011540052.1:c.3555C>T	XP_011538354.1:p.Val1185=
NM_022124.6:c.7032C>T MANE Select	NP_071407.4:p.Val2344=