Canonical Allele Identifier: CA2262378248

Gene: WNT3 LRRC37A2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46774013_46774014delinsAG , CM000679.2:g.46774013_46774014delinsAG	GRCh38
NC_000017.10:g.44851379_44851380delinsAG , CM000679.1:g.44851379_44851380delinsAG	GRCh37
NC_000017.9:g.42206542_42206543delinsAG	NCBI36
NG_008084.2:g.49703_49704delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-105_-115-104delinsCT (WNT3)	ENSP00000516418.1:n.-115-105_-115-104delinsCT
ENST00000225512.6:c.81-105_81-104delinsCT (WNT3) MANE Select	ENSP00000225512.5:n.81-105_81-104delinsCT
ENST00000225512.5:c.81-105_81-104delinsCT (WNT3)	ENSP00000225512.5:n.81-105_81-104delinsCT
ENST00000573788.5:n.492-105_492-104delinsCT (WNT3)
NM_030753.4:c.81-105_81-104delinsCT (WNT3)	NP_110380.1:n.81-105_81-104delinsCT
XM_024450773.1:c.4809+223494_4809+223495delinsAG (LRRC37A2)	XP_024306541.1:n.4809+223494_4809+223495delinsAG
NM_030753.5:c.81-105_81-104delinsCT (WNT3) MANE Select	NP_110380.1:n.81-105_81-104delinsCT