Canonical Allele Identifier: CA2638404170
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46774042_46774043insCCCGAGGTCAAAGGTAGC , CM000679.2:g.46774042_46774043insCCCGAGGTCAAAGGTAGC GRCh38
NC_000017.10:g.44851408_44851409insCCCGAGGTCAAAGGTAGC , CM000679.1:g.44851408_44851409insCCCGAGGTCAAAGGTAGC GRCh37
NC_000017.9:g.42206571_42206572insCCCGAGGTCAAAGGTAGC NCBI36
NG_008084.2:g.49674_49675insGCTACCTTTGACCTCGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-115-134_-115-133insGCTACCTTTGACCTCGGG (WNT3) ENSP00000516418.1:n.-115-134_-115-133insGCTACCTTTGACCTCGGG
ENST00000225512.6:c.81-134_81-133insGCTACCTTTGACCTCGGG (WNT3) MANE Select ENSP00000225512.5:n.81-134_81-133insGCTACCTTTGACCTCGGG
ENST00000225512.5:c.81-134_81-133insGCTACCTTTGACCTCGGG (WNT3) ENSP00000225512.5:n.81-134_81-133insGCTACCTTTGACCTCGGG
ENST00000573788.5:n.492-134_492-133insGCTACCTTTGACCTCGGG (WNT3)
NM_030753.4:c.81-134_81-133insGCTACCTTTGACCTCGGG (WNT3) NP_110380.1:n.81-134_81-133insGCTACCTTTGACCTCGGG
XM_024450773.1:c.4809+223523_4809+223524insCCCGAGGTCAAAGGTAGC (LRRC37A2) XP_024306541.1:n.4809+223523_4809+223524insCCCGAGGTCAAAGGTAGC...
NM_030753.5:c.81-134_81-133insGCTACCTTTGACCTCGGG (WNT3) MANE Select NP_110380.1:n.81-134_81-133insGCTACCTTTGACCTCGGG