Canonical Allele Identifier: CA377131285

Gene: CDH23

Linked Data

• dbSNP Id: rs201076440
• gnomAD v4: 10-71807518-G-C
• MyVariant Identifiers: chr10:g.73567275G>C (hg19) ; chr10:g.71807518G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807518G>C , CM000672.2:g.71807518G>C	GRCh38
NC_000010.10:g.73567275G>C , CM000672.1:g.73567275G>C	GRCh37
NC_000010.9:g.73237281G>C	NCBI36
NG_008835.1:g.415572G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8311G>C MANE Select	ENSP00000224721.9:p.Gly2771Arg
ENST00000642965.1:c.2244G>C	ENSP00000495222.1:n.2244G>C
ENST00000647092.1:c.1908G>C	ENSP00000495176.1:n.1908G>C
ENST00000224721.10:c.8326G>C	ENSP00000224721.8:p.Gly2776Arg
ENST00000398788.4:c.1591G>C	ENSP00000381768.3:p.Gly531Arg
ENST00000475158.1:n.1847G>C
ENST00000619887.4:c.1591G>C	ENSP00000478374.1:p.Gly531Arg
ENST00000622827.4:c.8311G>C	ENSP00000483211.1:p.Gly2771Arg
NM_001171933.1:c.1591G>C	NP_001165404.1:p.Gly531Arg
NM_001171934.1:c.1591G>C	NP_001165405.1:p.Gly531Arg
NM_022124.5:c.8311G>C	NP_071407.4:p.Gly2771Arg
XM_006717940.2:c.8506G>C	XP_006718003.1:p.Gly2836Arg
XM_006717942.2:c.8440G>C	XP_006718005.1:p.Gly2814Arg
XM_011540039.1:c.8503G>C	XP_011538341.1:p.Gly2835Arg
XM_011540040.1:c.8500G>C	XP_011538342.1:p.Gly2834Arg
XM_011540041.1:c.8446G>C	XP_011538343.1:p.Gly2816Arg
XM_011540042.1:c.8416G>C	XP_011538344.1:p.Gly2806Arg
XM_011540043.1:c.8506G>C	XP_011538345.1:p.Gly2836Arg
XM_011540044.1:c.8371G>C	XP_011538346.1:p.Gly2791Arg
XM_011540045.1:c.8506G>C	XP_011538347.1:p.Gly2836Arg
XM_011540046.1:c.7966G>C	XP_011538348.1:p.Gly2656Arg
XM_011540047.1:c.7324G>C	XP_011538349.1:p.Gly2442Arg
XM_011540052.1:c.4834G>C	XP_011538354.1:p.Gly1612Arg
NM_022124.6:c.8311G>C MANE Select	NP_071407.4:p.Gly2771Arg