Canonical Allele Identifier: CA2663173446

Gene: WNT10A

Linked Data

• gnomAD v4: 2-218882116-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882118del , CM000664.2:g.218882118del	GRCh38
NC_000002.11:g.219746840del , CM000664.1:g.219746840del	GRCh37
NC_000002.10:g.219455084del	NCBI36
NG_012179.1:g.6586del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-43del MANE Select	ENSP00000258411.3:n.114-43del
ENST00000258411.7:c.114-43del	ENSP00000258411.3:n.114-43del
NM_025216.2:c.114-43del	NP_079492.2:n.114-43del
XM_011511928.1:c.63-43del	XP_011510230.1:n.63-43del
XM_011511929.1:c.18-43del	XP_011510231.1:n.18-43del
XM_011511930.1:c.114-43del	XP_011510232.1:n.114-43del
XM_011511929.2:c.18-43del	XP_011510231.1:n.18-43del
NM_025216.3:c.114-43del MANE Select	NP_079492.2:n.114-43del