Canonical Allele Identifier: CA2843077851

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773623_46773638del , CM000679.2:g.46773623_46773638del	GRCh38
NC_000017.10:g.44850989_44851004del , CM000679.1:g.44850989_44851004del	GRCh37
NC_000017.9:g.42206152_42206167del	NCBI36
NG_008084.2:g.50082_50097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.127+33_127+48del (WNT3)	ENSP00000516418.1:n.127+33_127+48del
ENST00000225512.6:c.322+33_322+48del (WNT3) MANE Select	ENSP00000225512.5:n.322+33_322+48del
ENST00000225512.5:c.322+33_322+48del (WNT3)	ENSP00000225512.5:n.322+33_322+48del
NM_030753.4:c.322+33_322+48del (WNT3)	NP_110380.1:n.322+33_322+48del
XM_024450773.1:c.4809+223104_4809+223119del (LRRC37A2)	XP_024306541.1:n.4809+223104_4809+223119del
NM_030753.5:c.322+33_322+48del (WNT3) MANE Select	NP_110380.1:n.322+33_322+48del