Canonical Allele Identifier: CA350592266

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893195-A-G
• MyVariant Identifiers: chr2:g.219757917A>G (hg19) ; chr2:g.218893195A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893195A>G , CM000664.2:g.218893195A>G	GRCh38
NC_000002.11:g.219757917A>G , CM000664.1:g.219757917A>G	GRCh37
NC_000002.10:g.219466161A>G	NCBI36
NG_012179.1:g.17663A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1178A>G MANE Select	ENSP00000258411.3:p.His393Arg
ENST00000258411.7:c.1178A>G	ENSP00000258411.3:p.His393Arg
NM_025216.2:c.1178A>G	NP_079492.2:p.His393Arg
XM_011511928.1:c.1127A>G	XP_011510230.1:p.His376Arg
XM_011511929.1:c.1082A>G	XP_011510231.1:p.His361Arg
XM_011511930.1:c.798A>G	XP_011510232.1:p.Pro266=
XM_011511929.2:c.1082A>G	XP_011510231.1:p.His361Arg
NM_025216.3:c.1178A>G MANE Select	NP_079492.2:p.His393Arg