Canonical Allele Identifier: CA470062103

Gene: CDH23

Linked Data

• gnomAD v4: 10-71798520-C-T
• MyVariant Identifiers: chr10:g.73558277C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798520C>T , CM000672.2:g.71798520C>T	GRCh38
NC_000010.10:g.73558277C>T , CM000672.1:g.73558277C>T	GRCh37
NC_000010.9:g.73228283C>T	NCBI36
NG_008835.1:g.406574C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6996C>T MANE Select	ENSP00000224721.9:p.Thr2332=
ENST00000642965.1:c.929C>T	ENSP00000495222.1:n.929C>T
ENST00000647092.1:c.593C>T	ENSP00000495176.1:n.593C>T
ENST00000224721.10:c.7011C>T	ENSP00000224721.8:p.Thr2337=
ENST00000398788.4:c.276C>T	ENSP00000381768.3:p.Thr92=
ENST00000475158.1:n.532C>T
ENST00000619887.4:c.276C>T	ENSP00000478374.1:p.Thr92=
ENST00000622827.4:c.6996C>T	ENSP00000483211.1:p.Thr2332=
NM_001171933.1:c.276C>T	NP_001165404.1:p.Thr92=
NM_001171934.1:c.276C>T	NP_001165405.1:p.Thr92=
NM_022124.5:c.6996C>T	NP_071407.4:p.Thr2332=
XM_006717940.2:c.7191C>T	XP_006718003.1:p.Thr2397=
XM_006717942.2:c.7125C>T	XP_006718005.1:p.Thr2375=
XM_011540039.1:c.7188C>T	XP_011538341.1:p.Thr2396=
XM_011540040.1:c.7185C>T	XP_011538342.1:p.Thr2395=
XM_011540041.1:c.7131C>T	XP_011538343.1:p.Thr2377=
XM_011540042.1:c.7101C>T	XP_011538344.1:p.Thr2367=
XM_011540043.1:c.7191C>T	XP_011538345.1:p.Thr2397=
XM_011540044.1:c.7056C>T	XP_011538346.1:p.Thr2352=
XM_011540045.1:c.7191C>T	XP_011538347.1:p.Thr2397=
XM_011540046.1:c.6651C>T	XP_011538348.1:p.Thr2217=
XM_011540047.1:c.6009C>T	XP_011538349.1:p.Thr2003=
XM_011540052.1:c.3519C>T	XP_011538354.1:p.Thr1173=
NM_022124.6:c.6996C>T MANE Select	NP_071407.4:p.Thr2332=