Canonical Allele Identifier: CA645519891

Gene: WNT10A

Linked Data

• COSMIC: COSM1405526

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882274_218882275dup , CM000664.2:g.218882274_218882275dup	GRCh38
NC_000002.11:g.219746996_219746997dup , CM000664.1:g.219746996_219746997dup	GRCh37
NC_000002.10:g.219455240_219455241dup	NCBI36
NG_012179.1:g.6742_6743dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.227_228dup MANE Select	ENSP00000258411.3:p.Arg77CysfsTer?
ENST00000258411.7:c.227_228dup	ENSP00000258411.3:p.Arg77CysfsTer?
ENST00000458582.1:c.114_115dup
NM_025216.2:c.227_228dup	NP_079492.2:p.Arg77CysfsTer?
XM_011511928.1:c.176_177dup	XP_011510230.1:p.Arg60CysfsTer?
XM_011511929.1:c.131_132dup	XP_011510231.1:p.Arg45CysfsTer?
XM_011511930.1:c.227_228dup	XP_011510232.1:p.Arg77CysfsTer?
XM_011511929.2:c.131_132dup	XP_011510231.1:p.Arg45CysfsTer?
NM_025216.3:c.227_228dup MANE Select	NP_079492.2:p.Arg77CysfsTer?