Canonical Allele Identifier: CA470282384

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567277C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807520C>A , CM000672.2:g.71807520C>A	GRCh38
NC_000010.10:g.73567277C>A , CM000672.1:g.73567277C>A	GRCh37
NC_000010.9:g.73237283C>A	NCBI36
NG_008835.1:g.415574C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8313C>A MANE Select	ENSP00000224721.9:p.Gly2771=
ENST00000642965.1:c.2246C>A	ENSP00000495222.1:n.2246C>A
ENST00000647092.1:c.1910C>A	ENSP00000495176.1:n.1910C>A
ENST00000224721.10:c.8328C>A	ENSP00000224721.8:p.Gly2776=
ENST00000398788.4:c.1593C>A	ENSP00000381768.3:p.Gly531=
ENST00000475158.1:n.1849C>A
ENST00000619887.4:c.1593C>A	ENSP00000478374.1:p.Gly531=
ENST00000622827.4:c.8313C>A	ENSP00000483211.1:p.Gly2771=
NM_001171933.1:c.1593C>A	NP_001165404.1:p.Gly531=
NM_001171934.1:c.1593C>A	NP_001165405.1:p.Gly531=
NM_022124.5:c.8313C>A	NP_071407.4:p.Gly2771=
XM_006717940.2:c.8508C>A	XP_006718003.1:p.Gly2836=
XM_006717942.2:c.8442C>A	XP_006718005.1:p.Gly2814=
XM_011540039.1:c.8505C>A	XP_011538341.1:p.Gly2835=
XM_011540040.1:c.8502C>A	XP_011538342.1:p.Gly2834=
XM_011540041.1:c.8448C>A	XP_011538343.1:p.Gly2816=
XM_011540042.1:c.8418C>A	XP_011538344.1:p.Gly2806=
XM_011540043.1:c.8508C>A	XP_011538345.1:p.Gly2836=
XM_011540044.1:c.8373C>A	XP_011538346.1:p.Gly2791=
XM_011540045.1:c.8508C>A	XP_011538347.1:p.Gly2836=
XM_011540046.1:c.7968C>A	XP_011538348.1:p.Gly2656=
XM_011540047.1:c.7326C>A	XP_011538349.1:p.Gly2442=
XM_011540052.1:c.4836C>A	XP_011538354.1:p.Gly1612=
NM_022124.6:c.8313C>A MANE Select	NP_071407.4:p.Gly2771=