Canonical Allele Identifier: CA431417584

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 1658895
• ClinVar RCV Id: RCV002174421
• dbSNP Id: rs2106018848
• MyVariant Identifiers: chr2:g.219757903C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893181C>T , CM000664.2:g.218893181C>T	GRCh38
NC_000002.11:g.219757903C>T , CM000664.1:g.219757903C>T	GRCh37
NC_000002.10:g.219466147C>T	NCBI36
NG_012179.1:g.17649C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1164C>T MANE Select	ENSP00000258411.3:p.Arg388=
ENST00000258411.7:c.1164C>T	ENSP00000258411.3:p.Arg388=
NM_025216.2:c.1164C>T	NP_079492.2:p.Arg388=
XM_011511928.1:c.1113C>T	XP_011510230.1:p.Arg371=
XM_011511929.1:c.1068C>T	XP_011510231.1:p.Arg356=
XM_011511930.1:c.784C>T	XP_011510232.1:p.Gln262Ter
XM_011511929.2:c.1068C>T	XP_011510231.1:p.Arg356=
NM_025216.3:c.1164C>T MANE Select	NP_079492.2:p.Arg388=