Canonical Allele Identifier: CA470062486

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562744G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802987G>C , CM000672.2:g.71802987G>C	GRCh38
NC_000010.10:g.73562744G>C , CM000672.1:g.73562744G>C	GRCh37
NC_000010.9:g.73232750G>C	NCBI36
NG_008835.1:g.411041G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7572G>C MANE Select	ENSP00000224721.9:p.Ala2524=
ENST00000642965.1:c.1505G>C	ENSP00000495222.1:n.1505G>C
ENST00000647092.1:c.1169G>C	ENSP00000495176.1:n.1169G>C
ENST00000224721.10:c.7587G>C	ENSP00000224721.8:p.Ala2529=
ENST00000398788.4:c.852G>C	ENSP00000381768.3:p.Ala284=
ENST00000475158.1:n.1108G>C
ENST00000619887.4:c.852G>C	ENSP00000478374.1:p.Ala284=
ENST00000622827.4:c.7572G>C	ENSP00000483211.1:p.Ala2524=
NM_001171933.1:c.852G>C	NP_001165404.1:p.Ala284=
NM_001171934.1:c.852G>C	NP_001165405.1:p.Ala284=
NM_022124.5:c.7572G>C	NP_071407.4:p.Ala2524=
XM_006717940.2:c.7767G>C	XP_006718003.1:p.Ala2589=
XM_006717942.2:c.7701G>C	XP_006718005.1:p.Ala2567=
XM_011540039.1:c.7764G>C	XP_011538341.1:p.Ala2588=
XM_011540040.1:c.7761G>C	XP_011538342.1:p.Ala2587=
XM_011540041.1:c.7707G>C	XP_011538343.1:p.Ala2569=
XM_011540042.1:c.7677G>C	XP_011538344.1:p.Ala2559=
XM_011540043.1:c.7767G>C	XP_011538345.1:p.Ala2589=
XM_011540044.1:c.7632G>C	XP_011538346.1:p.Ala2544=
XM_011540045.1:c.7767G>C	XP_011538347.1:p.Ala2589=
XM_011540046.1:c.7227G>C	XP_011538348.1:p.Ala2409=
XM_011540047.1:c.6585G>C	XP_011538349.1:p.Ala2195=
XM_011540052.1:c.4095G>C	XP_011538354.1:p.Ala1365=
NM_022124.6:c.7572G>C MANE Select	NP_071407.4:p.Ala2524=