Canonical Allele Identifier: CA1328961336

Gene: WNT10A

Linked Data

• dbSNP Id: rs1944519790

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881771_218881772del , CM000664.2:g.218881771_218881772del	GRCh38
NC_000002.11:g.219746493_219746494del , CM000664.1:g.219746493_219746494del	GRCh37
NC_000002.10:g.219454737_219454738del	NCBI36
NG_012179.1:g.6239_6240del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-390_114-389del MANE Select	ENSP00000258411.3:n.114-390_114-389del
ENST00000258411.7:c.114-390_114-389del	ENSP00000258411.3:n.114-390_114-389del
NM_025216.2:c.114-390_114-389del	NP_079492.2:n.114-390_114-389del
XM_011511928.1:c.62+304_62+305del	XP_011510230.1:n.62+304_62+305del
XM_011511929.1:c.18-390_18-389del	XP_011510231.1:n.18-390_18-389del
XM_011511930.1:c.114-390_114-389del	XP_011510232.1:n.114-390_114-389del
XM_011511929.2:c.18-390_18-389del	XP_011510231.1:n.18-390_18-389del
NM_025216.3:c.114-390_114-389del MANE Select	NP_079492.2:n.114-390_114-389del