Canonical Allele Identifier: CA470062004

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558191C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798434C>A , CM000672.2:g.71798434C>A	GRCh38
NC_000010.10:g.73558191C>A , CM000672.1:g.73558191C>A	GRCh37
NC_000010.9:g.73228197C>A	NCBI36
NG_008835.1:g.406488C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6910C>A MANE Select	ENSP00000224721.9:p.Arg2304=
ENST00000642965.1:c.843C>A	ENSP00000495222.1:n.843C>A
ENST00000647092.1:c.507C>A	ENSP00000495176.1:n.507C>A
ENST00000224721.10:c.6925C>A	ENSP00000224721.8:p.Arg2309=
ENST00000398788.4:c.190C>A	ENSP00000381768.3:p.Arg64=
ENST00000475158.1:n.446C>A
ENST00000619887.4:c.190C>A	ENSP00000478374.1:p.Arg64=
ENST00000622827.4:c.6910C>A	ENSP00000483211.1:p.Arg2304=
NM_001171933.1:c.190C>A	NP_001165404.1:p.Arg64=
NM_001171934.1:c.190C>A	NP_001165405.1:p.Arg64=
NM_022124.5:c.6910C>A	NP_071407.4:p.Arg2304=
XM_006717940.2:c.7105C>A	XP_006718003.1:p.Arg2369=
XM_006717942.2:c.7039C>A	XP_006718005.1:p.Arg2347=
XM_011540039.1:c.7102C>A	XP_011538341.1:p.Arg2368=
XM_011540040.1:c.7099C>A	XP_011538342.1:p.Arg2367=
XM_011540041.1:c.7045C>A	XP_011538343.1:p.Arg2349=
XM_011540042.1:c.7015C>A	XP_011538344.1:p.Arg2339=
XM_011540043.1:c.7105C>A	XP_011538345.1:p.Arg2369=
XM_011540044.1:c.6970C>A	XP_011538346.1:p.Arg2324=
XM_011540045.1:c.7105C>A	XP_011538347.1:p.Arg2369=
XM_011540046.1:c.6565C>A	XP_011538348.1:p.Arg2189=
XM_011540047.1:c.5923C>A	XP_011538349.1:p.Arg1975=
XM_011540052.1:c.3433C>A	XP_011538354.1:p.Arg1145=
NM_022124.6:c.6910C>A MANE Select	NP_071407.4:p.Arg2304=