Canonical Allele Identifier: CA431234844
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757945G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893223G>T , CM000664.2:g.218893223G>T GRCh38
NC_000002.11:g.219757945G>T , CM000664.1:g.219757945G>T GRCh37
NC_000002.10:g.219466189G>T NCBI36
NG_012179.1:g.17691G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1206G>T MANE Select ENSP00000258411.3:p.Val402=
ENST00000258411.7:c.1206G>T ENSP00000258411.3:p.Val402=
ENST00000489887.1:n.3G>T
NM_025216.2:c.1206G>T NP_079492.2:p.Val402=
XM_011511928.1:c.1155G>T XP_011510230.1:p.Val385=
XM_011511929.1:c.1110G>T XP_011510231.1:p.Val370=
XM_011511930.1:c.826G>T XP_011510232.1:p.Gly276Cys
XM_011511929.2:c.1110G>T XP_011510231.1:p.Val370=
NM_025216.3:c.1206G>T MANE Select NP_079492.2:p.Val402=