Canonical Allele Identifier: CA350592464
Gene: WNT10A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.219757933G>C (hg19) chr2:g.218893211G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893211G>C , CM000664.2:g.218893211G>C GRCh38
NC_000002.11:g.219757933G>C , CM000664.1:g.219757933G>C GRCh37
NC_000002.10:g.219466177G>C NCBI36
NG_012179.1:g.17679G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1194G>C MANE Select ENSP00000258411.3:p.Trp398Cys
ENST00000258411.7:c.1194G>C ENSP00000258411.3:p.Trp398Cys
NM_025216.2:c.1194G>C NP_079492.2:p.Trp398Cys
XM_011511928.1:c.1143G>C XP_011510230.1:p.Trp381Cys
XM_011511929.1:c.1098G>C XP_011510231.1:p.Trp366Cys
XM_011511930.1:c.814G>C XP_011510232.1:p.Val272Leu
XM_011511929.2:c.1098G>C XP_011510231.1:p.Trp366Cys
NM_025216.3:c.1194G>C MANE Select NP_079492.2:p.Trp398Cys
Search 100 bp 5'
Search 100 bp 3'