Canonical Allele Identifier: CA2113853

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 1596370
• ClinVar RCV Id: RCV002113303
• dbSNP Id: rs765843965
• ExAC: 2:219746946 A / T
• gnomAD v2: 2-219746946-A-T
• gnomAD v4: 2-218882224-A-T
• MyVariant Identifiers: chr2:g.219746946A>T (hg19) ; chr2:g.218882224A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882224A>T , CM000664.2:g.218882224A>T	GRCh38
NC_000002.11:g.219746946A>T , CM000664.1:g.219746946A>T	GRCh37
NC_000002.10:g.219455190A>T	NCBI36
NG_012179.1:g.6692A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.177A>T MANE Select	ENSP00000258411.3:p.Thr59=
ENST00000258411.7:c.177A>T	ENSP00000258411.3:p.Thr59=
ENST00000458582.1:c.64A>T
NM_025216.2:c.177A>T	NP_079492.2:p.Thr59=
XM_011511928.1:c.126A>T	XP_011510230.1:p.Thr42=
XM_011511929.1:c.81A>T	XP_011510231.1:p.Thr27=
XM_011511930.1:c.177A>T	XP_011510232.1:p.Thr59=
XM_011511929.2:c.81A>T	XP_011510231.1:p.Thr27=
NM_025216.3:c.177A>T MANE Select	NP_079492.2:p.Thr59=