Canonical Allele Identifier: CA350618097

Gene: WNT10A

Linked Data

• dbSNP Id: rs1386895450
• gnomAD v4: 2-218882184-A-G
• MyVariant Identifiers: chr2:g.219746906A>G (hg19) ; chr2:g.218882184A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882184A>G , CM000664.2:g.218882184A>G	GRCh38
NC_000002.11:g.219746906A>G , CM000664.1:g.219746906A>G	GRCh37
NC_000002.10:g.219455150A>G	NCBI36
NG_012179.1:g.6652A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.137A>G MANE Select	ENSP00000258411.3:p.Asp46Gly
ENST00000258411.7:c.137A>G	ENSP00000258411.3:p.Asp46Gly
ENST00000458582.1:c.24A>G
NM_025216.2:c.137A>G	NP_079492.2:p.Asp46Gly
XM_011511928.1:c.86A>G	XP_011510230.1:p.Asp29Gly
XM_011511929.1:c.41A>G	XP_011510231.1:p.Asp14Gly
XM_011511930.1:c.137A>G	XP_011510232.1:p.Asp46Gly
XM_011511929.2:c.41A>G	XP_011510231.1:p.Asp14Gly
NM_025216.3:c.137A>G MANE Select	NP_079492.2:p.Asp46Gly