Canonical Allele Identifier: CA2262378105

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773651_46773653delinsCAG , CM000679.2:g.46773651_46773653delinsCAG	GRCh38
NC_000017.10:g.44851017_44851019delinsCAG , CM000679.1:g.44851017_44851019delinsCAG	GRCh37
NC_000017.9:g.42206180_42206182delinsCAG	NCBI36
NG_008084.2:g.50064_50066delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.127+15_127+17delinsCTG (WNT3)	ENSP00000516418.1:n.127+15_127+17delinsCTG
ENST00000225512.6:c.322+15_322+17delinsCTG (WNT3) MANE Select	ENSP00000225512.5:n.322+15_322+17delinsCTG
ENST00000225512.5:c.322+15_322+17delinsCTG (WNT3)	ENSP00000225512.5:n.322+15_322+17delinsCTG
NM_030753.4:c.322+15_322+17delinsCTG (WNT3)	NP_110380.1:n.322+15_322+17delinsCTG
XM_024450773.1:c.4809+223132_4809+223134delinsCAG (LRRC37A2)	XP_024306541.1:n.4809+223132_4809+223134delinsCAG
NM_030753.5:c.322+15_322+17delinsCTG (WNT3) MANE Select	NP_110380.1:n.322+15_322+17delinsCTG