Canonical Allele Identifier: CA377162333

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73565952C>G (hg19) ; chr10:g.71806195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806195C>G , CM000672.2:g.71806195C>G	GRCh38
NC_000010.10:g.73565952C>G , CM000672.1:g.73565952C>G	GRCh37
NC_000010.9:g.73235958C>G	NCBI36
NG_008835.1:g.414249C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8092C>G MANE Select	ENSP00000224721.9:p.Gln2698Glu
ENST00000642965.1:c.2025C>G	ENSP00000495222.1:n.2025C>G
ENST00000647092.1:c.1689C>G	ENSP00000495176.1:n.1689C>G
ENST00000224721.10:c.8107C>G	ENSP00000224721.8:p.Gln2703Glu
ENST00000398788.4:c.1372C>G	ENSP00000381768.3:p.Gln458Glu
ENST00000475158.1:n.1628C>G
ENST00000619887.4:c.1372C>G	ENSP00000478374.1:p.Gln458Glu
ENST00000622827.4:c.8092C>G	ENSP00000483211.1:p.Gln2698Glu
NM_001171933.1:c.1372C>G	NP_001165404.1:p.Gln458Glu
NM_001171934.1:c.1372C>G	NP_001165405.1:p.Gln458Glu
NM_022124.5:c.8092C>G	NP_071407.4:p.Gln2698Glu
XM_006717940.2:c.8287C>G	XP_006718003.1:p.Gln2763Glu
XM_006717942.2:c.8221C>G	XP_006718005.1:p.Gln2741Glu
XM_011540039.1:c.8284C>G	XP_011538341.1:p.Gln2762Glu
XM_011540040.1:c.8281C>G	XP_011538342.1:p.Gln2761Glu
XM_011540041.1:c.8227C>G	XP_011538343.1:p.Gln2743Glu
XM_011540042.1:c.8197C>G	XP_011538344.1:p.Gln2733Glu
XM_011540043.1:c.8287C>G	XP_011538345.1:p.Gln2763Glu
XM_011540044.1:c.8152C>G	XP_011538346.1:p.Gln2718Glu
XM_011540045.1:c.8287C>G	XP_011538347.1:p.Gln2763Glu
XM_011540046.1:c.7747C>G	XP_011538348.1:p.Gln2583Glu
XM_011540047.1:c.7105C>G	XP_011538349.1:p.Gln2369Glu
XM_011540052.1:c.4615C>G	XP_011538354.1:p.Gln1539Glu
NM_022124.6:c.8092C>G MANE Select	NP_071407.4:p.Gln2698Glu