Canonical Allele Identifier: CA350592207

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893188-C-G
• MyVariant Identifiers: chr2:g.219757910C>G (hg19) ; chr2:g.218893188C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893188C>G , CM000664.2:g.218893188C>G	GRCh38
NC_000002.11:g.219757910C>G , CM000664.1:g.219757910C>G	GRCh37
NC_000002.10:g.219466154C>G	NCBI36
NG_012179.1:g.17656C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1171C>G MANE Select	ENSP00000258411.3:p.Arg391Gly
ENST00000258411.7:c.1171C>G	ENSP00000258411.3:p.Arg391Gly
NM_025216.2:c.1171C>G	NP_079492.2:p.Arg391Gly
XM_011511928.1:c.1120C>G	XP_011510230.1:p.Arg374Gly
XM_011511929.1:c.1075C>G	XP_011510231.1:p.Arg359Gly
XM_011511930.1:c.791C>G	XP_011510232.1:p.Ala264Gly
XM_011511929.2:c.1075C>G	XP_011510231.1:p.Arg359Gly
NM_025216.3:c.1171C>G MANE Select	NP_079492.2:p.Arg391Gly