Canonical Allele Identifier: CA1328961379

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881873_218881874delinsTG , CM000664.2:g.218881873_218881874delinsTG	GRCh38
NC_000002.11:g.219746595_219746596delinsTG , CM000664.1:g.219746595_219746596delinsTG	GRCh37
NC_000002.10:g.219454839_219454840delinsTG	NCBI36
NG_012179.1:g.6341_6342delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-288_114-287delinsTG MANE Select	ENSP00000258411.3:n.114-288_114-287delinsTG
ENST00000258411.7:c.114-288_114-287delinsTG	ENSP00000258411.3:n.114-288_114-287delinsTG
NM_025216.2:c.114-288_114-287delinsTG	NP_079492.2:n.114-288_114-287delinsTG
XM_011511928.1:c.63-288_63-287delinsTG	XP_011510230.1:n.63-288_63-287delinsTG
XM_011511929.1:c.18-288_18-287delinsTG	XP_011510231.1:n.18-288_18-287delinsTG
XM_011511930.1:c.114-288_114-287delinsTG	XP_011510232.1:n.114-288_114-287delinsTG
XM_011511929.2:c.18-288_18-287delinsTG	XP_011510231.1:n.18-288_18-287delinsTG
NM_025216.3:c.114-288_114-287delinsTG MANE Select	NP_079492.2:n.114-288_114-287delinsTG