Canonical Allele Identifier: CA470061950

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558133G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798376G>T , CM000672.2:g.71798376G>T	GRCh38
NC_000010.10:g.73558133G>T , CM000672.1:g.73558133G>T	GRCh37
NC_000010.9:g.73228139G>T	NCBI36
NG_008835.1:g.406430G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6852G>T MANE Select	ENSP00000224721.9:p.Leu2284=
ENST00000642965.1:c.785G>T	ENSP00000495222.1:n.785G>T
ENST00000647092.1:c.449G>T	ENSP00000495176.1:n.449G>T
ENST00000224721.10:c.6867G>T	ENSP00000224721.8:p.Leu2289=
ENST00000398788.4:c.132G>T	ENSP00000381768.3:p.Leu44=
ENST00000475158.1:n.388G>T
ENST00000619887.4:c.132G>T	ENSP00000478374.1:p.Leu44=
ENST00000622827.4:c.6852G>T	ENSP00000483211.1:p.Leu2284=
NM_001171933.1:c.132G>T	NP_001165404.1:p.Leu44=
NM_001171934.1:c.132G>T	NP_001165405.1:p.Leu44=
NM_022124.5:c.6852G>T	NP_071407.4:p.Leu2284=
XM_006717940.2:c.7047G>T	XP_006718003.1:p.Leu2349=
XM_006717942.2:c.6981G>T	XP_006718005.1:p.Leu2327=
XM_011540039.1:c.7044G>T	XP_011538341.1:p.Leu2348=
XM_011540040.1:c.7041G>T	XP_011538342.1:p.Leu2347=
XM_011540041.1:c.6987G>T	XP_011538343.1:p.Leu2329=
XM_011540042.1:c.6957G>T	XP_011538344.1:p.Leu2319=
XM_011540043.1:c.7047G>T	XP_011538345.1:p.Leu2349=
XM_011540044.1:c.6912G>T	XP_011538346.1:p.Leu2304=
XM_011540045.1:c.7047G>T	XP_011538347.1:p.Leu2349=
XM_011540046.1:c.6507G>T	XP_011538348.1:p.Leu2169=
XM_011540047.1:c.5865G>T	XP_011538349.1:p.Leu1955=
XM_011540052.1:c.3375G>T	XP_011538354.1:p.Leu1125=
NM_022124.6:c.6852G>T MANE Select	NP_071407.4:p.Leu2284=