Canonical Allele Identifier: CA2836836001

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773617_46773618insGGGCGGGGGGG , CM000679.2:g.46773617_46773618insGGGCGGGGGGG	GRCh38
NC_000017.10:g.44850983_44850984insGGGCGGGGGGG , CM000679.1:g.44850983_44850984insGGGCGGGGGGG	GRCh37
NC_000017.9:g.42206146_42206147insGGGCGGGGGGG	NCBI36
NG_008084.2:g.50100_50101insCCCCCCGCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.127+51_127+52insCCCCCCGCCCC (WNT3)	ENSP00000516418.1:n.127+51_127+52insCCCCCCGCCCC
ENST00000225512.6:c.322+51_322+52insCCCCCCGCCCC (WNT3) MANE Select	ENSP00000225512.5:n.322+51_322+52insCCCCCCGCCCC
ENST00000225512.5:c.322+51_322+52insCCCCCCGCCCC (WNT3)	ENSP00000225512.5:n.322+51_322+52insCCCCCCGCCCC
NM_030753.4:c.322+51_322+52insCCCCCCGCCCC (WNT3)	NP_110380.1:n.322+51_322+52insCCCCCCGCCCC
XM_024450773.1:c.4809+223098_4809+223099insGGGCGGGGGGG (LRRC37A2)	XP_024306541.1:n.4809+223098_4809+223099insGGGCGGGGGGG
NM_030753.5:c.322+51_322+52insCCCCCCGCCCC (WNT3) MANE Select	NP_110380.1:n.322+51_322+52insCCCCCCGCCCC