Canonical Allele Identifier: CA350592463

Gene: WNT10A

Linked Data

• dbSNP Id: rs1381228558
• gnomAD v2: 2-219757933-G-A
• gnomAD v4: 2-218893211-G-A
• MyVariant Identifiers: chr2:g.219757933G>A (hg19) ; chr2:g.218893211G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1194G>A MANE Select	ENSP00000258411.3:p.Trp398Ter
ENST00000258411.7:c.1194G>A	ENSP00000258411.3:p.Trp398Ter
NM_025216.2:c.1194G>A	NP_079492.2:p.Trp398Ter
XM_011511928.1:c.1143G>A	XP_011510230.1:p.Trp381Ter
XM_011511929.1:c.1098G>A	XP_011510231.1:p.Trp366Ter
XM_011511930.1:c.814G>A	XP_011510232.1:p.Val272Met
XM_011511929.2:c.1098G>A	XP_011510231.1:p.Trp366Ter
NM_025216.3:c.1194G>A MANE Select	NP_079492.2:p.Trp398Ter