Canonical Allele Identifier: CA350618135

Gene: WNT10A

Linked Data

• dbSNP Id: rs1283156128
• gnomAD v2: 2-219746914-C-A
• gnomAD v4: 2-218882192-C-A
• MyVariant Identifiers: chr2:g.219746914C>A (hg19) ; chr2:g.218882192C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882192C>A , CM000664.2:g.218882192C>A	GRCh38
NC_000002.11:g.219746914C>A , CM000664.1:g.219746914C>A	GRCh37
NC_000002.10:g.219455158C>A	NCBI36
NG_012179.1:g.6660C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.145C>A MANE Select	ENSP00000258411.3:p.Leu49Ile
ENST00000258411.7:c.145C>A	ENSP00000258411.3:p.Leu49Ile
ENST00000458582.1:c.32C>A
NM_025216.2:c.145C>A	NP_079492.2:p.Leu49Ile
XM_011511928.1:c.94C>A	XP_011510230.1:p.Leu32Ile
XM_011511929.1:c.49C>A	XP_011510231.1:p.Leu17Ile
XM_011511930.1:c.145C>A	XP_011510232.1:p.Leu49Ile
XM_011511929.2:c.49C>A	XP_011510231.1:p.Leu17Ile
NM_025216.3:c.145C>A MANE Select	NP_079492.2:p.Leu49Ile