Canonical Allele Identifier: CA2638404184

Gene: WNT3 LRRC37A2

Linked Data

• gnomAD v4: 17-46774056-G-GCCCCTCAAAGCGCCCCTCAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46774056_46774057insCCCCTCAAAGCGCCCCTCAAA , CM000679.2:g.46774056_46774057insCCCCTCAAAGCGCCCCTCAAA	GRCh38
NC_000017.10:g.44851422_44851423insCCCCTCAAAGCGCCCCTCAAA , CM000679.1:g.44851422_44851423insCCCCTCAAAGCGCCCCTCAAA	GRCh37
NC_000017.9:g.42206585_42206586insCCCCTCAAAGCGCCCCTCAAA	NCBI36
NG_008084.2:g.49660_49661insTTTGAGGGGCGCTTTGAGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706495.1:c.-115-148_-115-147insTTTGAGGGGCGCTTTGAGGGG (WNT3)	ENSP00000516418.1:n.-115-148_-115-147insTTTGAGGGGCGCTTTGAGGGG...
ENST00000225512.6:c.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG (WNT3) MANE Select	ENSP00000225512.5:n.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG
ENST00000225512.5:c.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG (WNT3)	ENSP00000225512.5:n.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG
ENST00000573788.5:n.492-148_492-147insTTTGAGGGGCGCTTTGAGGGG (WNT3)
NM_030753.4:c.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG (WNT3)	NP_110380.1:n.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG
XM_024450773.1:c.4809+223537_4809+223538insCCCCTCAAAGCGCCCCTCAAA (LRRC37A2)	XP_024306541.1:n.4809+223537_4809+223538insCCCCTCAAAGCGCCCCTC...
NM_030753.5:c.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG (WNT3) MANE Select	NP_110380.1:n.81-148_81-147insTTTGAGGGGCGCTTTGAGGGG