Canonical Allele Identifier: CA377158116

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558257G>C (hg19) ; chr10:g.71798500G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798500G>C , CM000672.2:g.71798500G>C	GRCh38
NC_000010.10:g.73558257G>C , CM000672.1:g.73558257G>C	GRCh37
NC_000010.9:g.73228263G>C	NCBI36
NG_008835.1:g.406554G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6976G>C MANE Select	ENSP00000224721.9:p.Gly2326Arg
ENST00000642965.1:c.909G>C	ENSP00000495222.1:n.909G>C
ENST00000647092.1:c.573G>C	ENSP00000495176.1:n.573G>C
ENST00000224721.10:c.6991G>C	ENSP00000224721.8:p.Gly2331Arg
ENST00000398788.4:c.256G>C	ENSP00000381768.3:p.Gly86Arg
ENST00000475158.1:n.512G>C
ENST00000619887.4:c.256G>C	ENSP00000478374.1:p.Gly86Arg
ENST00000622827.4:c.6976G>C	ENSP00000483211.1:p.Gly2326Arg
NM_001171933.1:c.256G>C	NP_001165404.1:p.Gly86Arg
NM_001171934.1:c.256G>C	NP_001165405.1:p.Gly86Arg
NM_022124.5:c.6976G>C	NP_071407.4:p.Gly2326Arg
XM_006717940.2:c.7171G>C	XP_006718003.1:p.Gly2391Arg
XM_006717942.2:c.7105G>C	XP_006718005.1:p.Gly2369Arg
XM_011540039.1:c.7168G>C	XP_011538341.1:p.Gly2390Arg
XM_011540040.1:c.7165G>C	XP_011538342.1:p.Gly2389Arg
XM_011540041.1:c.7111G>C	XP_011538343.1:p.Gly2371Arg
XM_011540042.1:c.7081G>C	XP_011538344.1:p.Gly2361Arg
XM_011540043.1:c.7171G>C	XP_011538345.1:p.Gly2391Arg
XM_011540044.1:c.7036G>C	XP_011538346.1:p.Gly2346Arg
XM_011540045.1:c.7171G>C	XP_011538347.1:p.Gly2391Arg
XM_011540046.1:c.6631G>C	XP_011538348.1:p.Gly2211Arg
XM_011540047.1:c.5989G>C	XP_011538349.1:p.Gly1997Arg
XM_011540052.1:c.3499G>C	XP_011538354.1:p.Gly1167Arg
NM_022124.6:c.6976G>C MANE Select	NP_071407.4:p.Gly2326Arg