Canonical Allele Identifier: CA2113849

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 1082175
• ClinVar RCV Id: RCV001398399
• dbSNP Id: rs143421847
• ExAC: 2:219746928 C / T
• gnomAD v2: 2-219746928-C-T
• gnomAD v3: 2-218882206-C-T
• gnomAD v4: 2-218882206-C-T
• COSMIC: COSM4091546
• MyVariant Identifiers: chr2:g.219746928C>T (hg19) ; chr2:g.218882206C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882206C>T , CM000664.2:g.218882206C>T	GRCh38
NC_000002.11:g.219746928C>T , CM000664.1:g.219746928C>T	GRCh37
NC_000002.10:g.219455172C>T	NCBI36
NG_012179.1:g.6674C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.159C>T MANE Select	ENSP00000258411.3:p.Pro53=
ENST00000258411.7:c.159C>T	ENSP00000258411.3:p.Pro53=
ENST00000458582.1:c.46C>T
NM_025216.2:c.159C>T	NP_079492.2:p.Pro53=
XM_011511928.1:c.108C>T	XP_011510230.1:p.Pro36=
XM_011511929.1:c.63C>T	XP_011510231.1:p.Pro21=
XM_011511930.1:c.159C>T	XP_011510232.1:p.Pro53=
XM_011511929.2:c.63C>T	XP_011510231.1:p.Pro21=
NM_025216.3:c.159C>T MANE Select	NP_079492.2:p.Pro53=