Canonical Allele Identifier: CA377162331

Gene: CDH23

Linked Data

• gnomAD v4: 10-71806195-C-A
• MyVariant Identifiers: chr10:g.73565952C>A (hg19) ; chr10:g.71806195C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8092C>A MANE Select	ENSP00000224721.9:p.Gln2698Lys
ENST00000642965.1:c.2025C>A	ENSP00000495222.1:n.2025C>A
ENST00000647092.1:c.1689C>A	ENSP00000495176.1:n.1689C>A
ENST00000224721.10:c.8107C>A	ENSP00000224721.8:p.Gln2703Lys
ENST00000398788.4:c.1372C>A	ENSP00000381768.3:p.Gln458Lys
ENST00000475158.1:n.1628C>A
ENST00000619887.4:c.1372C>A	ENSP00000478374.1:p.Gln458Lys
ENST00000622827.4:c.8092C>A	ENSP00000483211.1:p.Gln2698Lys
NM_001171933.1:c.1372C>A	NP_001165404.1:p.Gln458Lys
NM_001171934.1:c.1372C>A	NP_001165405.1:p.Gln458Lys
NM_022124.5:c.8092C>A	NP_071407.4:p.Gln2698Lys
XM_006717940.2:c.8287C>A	XP_006718003.1:p.Gln2763Lys
XM_006717942.2:c.8221C>A	XP_006718005.1:p.Gln2741Lys
XM_011540039.1:c.8284C>A	XP_011538341.1:p.Gln2762Lys
XM_011540040.1:c.8281C>A	XP_011538342.1:p.Gln2761Lys
XM_011540041.1:c.8227C>A	XP_011538343.1:p.Gln2743Lys
XM_011540042.1:c.8197C>A	XP_011538344.1:p.Gln2733Lys
XM_011540043.1:c.8287C>A	XP_011538345.1:p.Gln2763Lys
XM_011540044.1:c.8152C>A	XP_011538346.1:p.Gln2718Lys
XM_011540045.1:c.8287C>A	XP_011538347.1:p.Gln2763Lys
XM_011540046.1:c.7747C>A	XP_011538348.1:p.Gln2583Lys
XM_011540047.1:c.7105C>A	XP_011538349.1:p.Gln2369Lys
XM_011540052.1:c.4615C>A	XP_011538354.1:p.Gln1539Lys
NM_022124.6:c.8092C>A MANE Select	NP_071407.4:p.Gln2698Lys