Canonical Allele Identifier: CA470069194

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500596A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740839A>C , CM000672.2:g.71740839A>C	GRCh38
NC_000010.10:g.73500596A>C , CM000672.1:g.73500596A>C	GRCh37
NC_000010.9:g.73170602A>C	NCBI36
NG_008835.1:g.348893A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4506A>C MANE Select	ENSP00000224721.9:p.Arg1502=
ENST00000224721.10:c.4521A>C	ENSP00000224721.8:p.Arg1507=
ENST00000398792.3:n.1195A>C
ENST00000622827.4:c.4506A>C	ENSP00000483211.1:p.Arg1502=
NM_022124.5:c.4506A>C	NP_071407.4:p.Arg1502=
XM_006717940.2:c.4701A>C	XP_006718003.1:p.Arg1567=
XM_006717942.2:c.4635A>C	XP_006718005.1:p.Arg1545=
XM_011540039.1:c.4698A>C	XP_011538341.1:p.Arg1566=
XM_011540040.1:c.4695A>C	XP_011538342.1:p.Arg1565=
XM_011540041.1:c.4641A>C	XP_011538343.1:p.Arg1547=
XM_011540042.1:c.4701A>C	XP_011538344.1:p.Arg1567=
XM_011540043.1:c.4701A>C	XP_011538345.1:p.Arg1567=
XM_011540044.1:c.4566A>C	XP_011538346.1:p.Arg1522=
XM_011540045.1:c.4701A>C	XP_011538347.1:p.Arg1567=
XM_011540046.1:c.4161A>C	XP_011538348.1:p.Arg1387=
XM_011540047.1:c.3519A>C	XP_011538349.1:p.Arg1173=
XM_011540048.1:c.4701A>C	XP_011538350.1:p.Arg1567=
XM_011540049.1:c.4701A>C	XP_011538351.1:p.Arg1567=
XM_011540050.1:c.4701A>C	XP_011538352.1:p.Arg1567=
XM_011540051.1:c.4701A>C	XP_011538353.1:p.Arg1567=
XM_011540052.1:c.1029A>C	XP_011538354.1:p.Arg343=
XM_011540053.1:c.4701A>C	XP_011538355.1:p.Arg1567=
XR_945796.1:n.4944A>C
NM_022124.6:c.4506A>C MANE Select	NP_071407.4:p.Arg1502=