Canonical Allele Identifier: CA350592773
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757971A>C (hg19) chr2:g.218893249A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893249A>C , CM000664.2:g.218893249A>C GRCh38
NC_000002.11:g.219757971A>C , CM000664.1:g.219757971A>C GRCh37
NC_000002.10:g.219466215A>C NCBI36
NG_012179.1:g.17717A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1232A>C MANE Select ENSP00000258411.3:p.Glu411Ala
ENST00000258411.7:c.1232A>C ENSP00000258411.3:p.Glu411Ala
ENST00000489887.1:n.29A>C
NM_025216.2:c.1232A>C NP_079492.2:p.Glu411Ala
XM_011511928.1:c.1181A>C XP_011510230.1:p.Glu394Ala
XM_011511929.1:c.1136A>C XP_011510231.1:p.Glu379Ala
XM_011511930.1:c.852A>C XP_011510232.1:p.Arg284=
XM_011511929.2:c.1136A>C XP_011510231.1:p.Glu379Ala
NM_025216.3:c.1232A>C MANE Select NP_079492.2:p.Glu411Ala
Search 100 bp 5'
Search 100 bp 3'