Canonical Allele Identifier: CA2663174684

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218893382-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893382T>G , CM000664.2:g.218893382T>G	GRCh38
NC_000002.11:g.219758104T>G , CM000664.1:g.219758104T>G	GRCh37
NC_000002.10:g.219466348T>G	NCBI36
NG_012179.1:g.17850T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.*111T>G MANE Select	ENSP00000258411.3:n.*111T>G
ENST00000258411.7:c.*111T>G	ENSP00000258411.3:n.*111T>G
ENST00000489887.1:n.47+115T>G
NM_025216.2:c.*111T>G	NP_079492.2:n.*111T>G
XM_011511928.1:c.*111T>G	XP_011510230.1:n.*111T>G
XM_011511929.1:c.*111T>G	XP_011510231.1:n.*111T>G
XM_011511930.1:c.*85T>G	XP_011510232.1:n.*85T>G
XM_011511929.2:c.*111T>G	XP_011510231.1:n.*111T>G
NM_025216.3:c.*111T>G MANE Select	NP_079492.2:n.*111T>G