Canonical Allele Identifier: CA431416422
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219746925G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218882203G>A , CM000664.2:g.218882203G>A GRCh38
NC_000002.11:g.219746925G>A , CM000664.1:g.219746925G>A GRCh37
NC_000002.10:g.219455169G>A NCBI36
NG_012179.1:g.6671G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.156G>A MANE Select ENSP00000258411.3:p.Glu52=
ENST00000258411.7:c.156G>A ENSP00000258411.3:p.Glu52=
ENST00000458582.1:c.43G>A
NM_025216.2:c.156G>A NP_079492.2:p.Glu52=
XM_011511928.1:c.105G>A XP_011510230.1:p.Glu35=
XM_011511929.1:c.60G>A XP_011510231.1:p.Glu20=
XM_011511930.1:c.156G>A XP_011510232.1:p.Glu52=
XM_011511929.2:c.60G>A XP_011510231.1:p.Glu20=
NM_025216.3:c.156G>A MANE Select NP_079492.2:p.Glu52=