Canonical Allele Identifier: CA350592155

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893182-A-T
• MyVariant Identifiers: chr2:g.219757904A>T (hg19) ; chr2:g.218893182A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893182A>T , CM000664.2:g.218893182A>T	GRCh38
NC_000002.11:g.219757904A>T , CM000664.1:g.219757904A>T	GRCh37
NC_000002.10:g.219466148A>T	NCBI36
NG_012179.1:g.17650A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1165A>T MANE Select	ENSP00000258411.3:p.Ser389Cys
ENST00000258411.7:c.1165A>T	ENSP00000258411.3:p.Ser389Cys
NM_025216.2:c.1165A>T	NP_079492.2:p.Ser389Cys
XM_011511928.1:c.1114A>T	XP_011510230.1:p.Ser372Cys
XM_011511929.1:c.1069A>T	XP_011510231.1:p.Ser357Cys
XM_011511930.1:c.785A>T	XP_011510232.1:p.Gln262Leu
XM_011511929.2:c.1069A>T	XP_011510231.1:p.Ser357Cys
NM_025216.3:c.1165A>T MANE Select	NP_079492.2:p.Ser389Cys