Canonical Allele Identifier: CA431416455

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 1087529
• ClinVar RCV Id: RCV001405688
• dbSNP Id: rs904675306
• gnomAD v4: 2-218882248-G-A
• MyVariant Identifiers: chr2:g.219746970G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882248G>A , CM000664.2:g.218882248G>A	GRCh38
NC_000002.11:g.219746970G>A , CM000664.1:g.219746970G>A	GRCh37
NC_000002.10:g.219455214G>A	NCBI36
NG_012179.1:g.6716G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.201G>A MANE Select	ENSP00000258411.3:p.Leu67=
ENST00000258411.7:c.201G>A	ENSP00000258411.3:p.Leu67=
ENST00000458582.1:c.88G>A
NM_025216.2:c.201G>A	NP_079492.2:p.Leu67=
XM_011511928.1:c.150G>A	XP_011510230.1:p.Leu50=
XM_011511929.1:c.105G>A	XP_011510231.1:p.Leu35=
XM_011511930.1:c.201G>A	XP_011510232.1:p.Leu67=
XM_011511929.2:c.105G>A	XP_011510231.1:p.Leu35=
NM_025216.3:c.201G>A MANE Select	NP_079492.2:p.Leu67=