Canonical Allele Identifier: CA1328961333

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881765_218881767delinsTTG , CM000664.2:g.218881765_218881767delinsTTG	GRCh38
NC_000002.11:g.219746487_219746489delinsTTG , CM000664.1:g.219746487_219746489delinsTTG	GRCh37
NC_000002.10:g.219454731_219454733delinsTTG	NCBI36
NG_012179.1:g.6233_6235delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-396_114-394delinsTTG MANE Select	ENSP00000258411.3:n.114-396_114-394delinsTTG
ENST00000258411.7:c.114-396_114-394delinsTTG	ENSP00000258411.3:n.114-396_114-394delinsTTG
NM_025216.2:c.114-396_114-394delinsTTG	NP_079492.2:n.114-396_114-394delinsTTG
XM_011511928.1:c.62+298_62+300delinsTTG	XP_011510230.1:n.62+298_62+300delinsTTG
XM_011511929.1:c.18-396_18-394delinsTTG	XP_011510231.1:n.18-396_18-394delinsTTG
XM_011511930.1:c.114-396_114-394delinsTTG	XP_011510232.1:n.114-396_114-394delinsTTG
XM_011511929.2:c.18-396_18-394delinsTTG	XP_011510231.1:n.18-396_18-394delinsTTG
NM_025216.3:c.114-396_114-394delinsTTG MANE Select	NP_079492.2:n.114-396_114-394delinsTTG