Canonical Allele Identifier: CA431417591

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 2930676
• ClinVar RCV Id: RCV003789986
• gnomAD v4: 2-218893184-C-T
• MyVariant Identifiers: chr2:g.219757906C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893184C>T , CM000664.2:g.218893184C>T	GRCh38
NC_000002.11:g.219757906C>T , CM000664.1:g.219757906C>T	GRCh37
NC_000002.10:g.219466150C>T	NCBI36
NG_012179.1:g.17652C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1167C>T MANE Select	ENSP00000258411.3:p.Ser389=
ENST00000258411.7:c.1167C>T	ENSP00000258411.3:p.Ser389=
NM_025216.2:c.1167C>T	NP_079492.2:p.Ser389=
XM_011511928.1:c.1116C>T	XP_011510230.1:p.Ser372=
XM_011511929.1:c.1071C>T	XP_011510231.1:p.Ser357=
XM_011511930.1:c.787C>T	XP_011510232.1:p.Arg263Ter
XM_011511929.2:c.1071C>T	XP_011510231.1:p.Ser357=
NM_025216.3:c.1167C>T MANE Select	NP_079492.2:p.Ser389=