Canonical Allele Identifier: CA350618144

Gene: WNT10A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.145C>T MANE Select	ENSP00000258411.3:p.Leu49Phe
ENST00000258411.7:c.145C>T	ENSP00000258411.3:p.Leu49Phe
ENST00000458582.1:c.32C>T
NM_025216.2:c.145C>T	NP_079492.2:p.Leu49Phe
XM_011511928.1:c.94C>T	XP_011510230.1:p.Leu32Phe
XM_011511929.1:c.49C>T	XP_011510231.1:p.Leu17Phe
XM_011511930.1:c.145C>T	XP_011510232.1:p.Leu49Phe
XM_011511929.2:c.49C>T	XP_011510231.1:p.Leu17Phe
NM_025216.3:c.145C>T MANE Select	NP_079492.2:p.Leu49Phe