Canonical Allele Identifier: CA431417577

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 1115370
• ClinVar RCV Id: RCV001443363
• dbSNP Id: rs1464589833
• gnomAD v4: 2-218893178-G-T
• MyVariant Identifiers: chr2:g.219757900G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893178G>T , CM000664.2:g.218893178G>T	GRCh38
NC_000002.11:g.219757900G>T , CM000664.1:g.219757900G>T	GRCh37
NC_000002.10:g.219466144G>T	NCBI36
NG_012179.1:g.17646G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1161G>T MANE Select	ENSP00000258411.3:p.Thr387=
ENST00000258411.7:c.1161G>T	ENSP00000258411.3:p.Thr387=
NM_025216.2:c.1161G>T	NP_079492.2:p.Thr387=
XM_011511928.1:c.1110G>T	XP_011510230.1:p.Thr370=
XM_011511929.1:c.1065G>T	XP_011510231.1:p.Thr355=
XM_011511930.1:c.781G>T	XP_011510232.1:p.Ala261Ser
XM_011511929.2:c.1065G>T	XP_011510231.1:p.Thr355=
NM_025216.3:c.1161G>T MANE Select	NP_079492.2:p.Thr387=