Canonical Allele Identifier: CA377157763

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558155C>A (hg19) ; chr10:g.71798398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798398C>A , CM000672.2:g.71798398C>A	GRCh38
NC_000010.10:g.73558155C>A , CM000672.1:g.73558155C>A	GRCh37
NC_000010.9:g.73228161C>A	NCBI36
NG_008835.1:g.406452C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6874C>A MANE Select	ENSP00000224721.9:p.Gln2292Lys
ENST00000642965.1:c.807C>A	ENSP00000495222.1:n.807C>A
ENST00000647092.1:c.471C>A	ENSP00000495176.1:n.471C>A
ENST00000224721.10:c.6889C>A	ENSP00000224721.8:p.Gln2297Lys
ENST00000398788.4:c.154C>A	ENSP00000381768.3:p.Gln52Lys
ENST00000475158.1:n.410C>A
ENST00000619887.4:c.154C>A	ENSP00000478374.1:p.Gln52Lys
ENST00000622827.4:c.6874C>A	ENSP00000483211.1:p.Gln2292Lys
NM_001171933.1:c.154C>A	NP_001165404.1:p.Gln52Lys
NM_001171934.1:c.154C>A	NP_001165405.1:p.Gln52Lys
NM_022124.5:c.6874C>A	NP_071407.4:p.Gln2292Lys
XM_006717940.2:c.7069C>A	XP_006718003.1:p.Gln2357Lys
XM_006717942.2:c.7003C>A	XP_006718005.1:p.Gln2335Lys
XM_011540039.1:c.7066C>A	XP_011538341.1:p.Gln2356Lys
XM_011540040.1:c.7063C>A	XP_011538342.1:p.Gln2355Lys
XM_011540041.1:c.7009C>A	XP_011538343.1:p.Gln2337Lys
XM_011540042.1:c.6979C>A	XP_011538344.1:p.Gln2327Lys
XM_011540043.1:c.7069C>A	XP_011538345.1:p.Gln2357Lys
XM_011540044.1:c.6934C>A	XP_011538346.1:p.Gln2312Lys
XM_011540045.1:c.7069C>A	XP_011538347.1:p.Gln2357Lys
XM_011540046.1:c.6529C>A	XP_011538348.1:p.Gln2177Lys
XM_011540047.1:c.5887C>A	XP_011538349.1:p.Gln1963Lys
XM_011540052.1:c.3397C>A	XP_011538354.1:p.Gln1133Lys
NM_022124.6:c.6874C>A MANE Select	NP_071407.4:p.Gln2292Lys