Canonical Allele Identifier: CA2262378257
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46774028G= , CM000679.2:g.46774028G= GRCh38
NC_000017.10:g.44851394G= , CM000679.1:g.44851394G= GRCh37
NC_000017.9:g.42206557G= NCBI36
NG_008084.2:g.49689C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-115-119C= (WNT3) ENSP00000516418.1:n.-115-119C=
ENST00000225512.6:c.81-119C= (WNT3) MANE Select ENSP00000225512.5:n.81-119C=
ENST00000225512.5:c.81-119C= (WNT3) ENSP00000225512.5:n.81-119C=
ENST00000573788.5:n.492-119C= (WNT3)
NM_030753.4:c.81-119C= (WNT3) NP_110380.1:n.81-119C=
XM_024450773.1:c.4809+223509G= (LRRC37A2) XP_024306541.1:n.4809+223509G=
NM_030753.5:c.81-119C= (WNT3) MANE Select NP_110380.1:n.81-119C=