Canonical Allele Identifier: CA2638404072

Gene: WNT3 LRRC37A2

Linked Data

• gnomAD v4: 17-46773913-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46773914dup , CM000679.2:g.46773914dup	GRCh38
NC_000017.10:g.44851280dup , CM000679.1:g.44851280dup	GRCh37
NC_000017.9:g.42206443dup	NCBI36
NG_008084.2:g.49803dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-5dup (WNT3)	ENSP00000516418.1:n.-115-5dup
ENST00000225512.6:c.81-5dup (WNT3) MANE Select	ENSP00000225512.5:n.81-5dup
ENST00000225512.5:c.81-5dup (WNT3)	ENSP00000225512.5:n.81-5dup
ENST00000573788.5:n.492-5dup (WNT3)
NM_030753.4:c.81-5dup (WNT3)	NP_110380.1:n.81-5dup
XM_024450773.1:c.4809+223395dup (LRRC37A2)	XP_024306541.1:n.4809+223395dup
NM_030753.5:c.81-5dup (WNT3) MANE Select	NP_110380.1:n.81-5dup