Canonical Allele Identifier: CA431234831

Gene: WNT10A

Linked Data

• ClinVar Variation Id: 753608
• ClinVar RCV Id: RCV001488970
• dbSNP Id: rs1575235198
• MyVariant Identifiers: chr2:g.219757912C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893190C>T , CM000664.2:g.218893190C>T	GRCh38
NC_000002.11:g.219757912C>T , CM000664.1:g.219757912C>T	GRCh37
NC_000002.10:g.219466156C>T	NCBI36
NG_012179.1:g.17658C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1173C>T MANE Select	ENSP00000258411.3:p.Arg391=
ENST00000258411.7:c.1173C>T	ENSP00000258411.3:p.Arg391=
NM_025216.2:c.1173C>T	NP_079492.2:p.Arg391=
XM_011511928.1:c.1122C>T	XP_011510230.1:p.Arg374=
XM_011511929.1:c.1077C>T	XP_011510231.1:p.Arg359=
XM_011511930.1:c.793C>T	XP_011510232.1:p.Leu265=
XM_011511929.2:c.1077C>T	XP_011510231.1:p.Arg359=
NM_025216.3:c.1173C>T MANE Select	NP_079492.2:p.Arg391=