Canonical Allele Identifier: CA2262378207

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773921_46773923delinsCAG , CM000679.2:g.46773921_46773923delinsCAG	GRCh38
NC_000017.10:g.44851287_44851289delinsCAG , CM000679.1:g.44851287_44851289delinsCAG	GRCh37
NC_000017.9:g.42206450_42206452delinsCAG	NCBI36
NG_008084.2:g.49794_49796delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-14_-115-12delinsCTG (WNT3)	ENSP00000516418.1:n.-115-14_-115-12delinsCTG
ENST00000225512.6:c.81-14_81-12delinsCTG (WNT3) MANE Select	ENSP00000225512.5:n.81-14_81-12delinsCTG
ENST00000225512.5:c.81-14_81-12delinsCTG (WNT3)	ENSP00000225512.5:n.81-14_81-12delinsCTG
ENST00000573788.5:n.492-14_492-12delinsCTG (WNT3)
NM_030753.4:c.81-14_81-12delinsCTG (WNT3)	NP_110380.1:n.81-14_81-12delinsCTG
XM_024450773.1:c.4809+223402_4809+223404delinsCAG (LRRC37A2)	XP_024306541.1:n.4809+223402_4809+223404delinsCAG
NM_030753.5:c.81-14_81-12delinsCTG (WNT3) MANE Select	NP_110380.1:n.81-14_81-12delinsCTG