Canonical Allele Identifier: CA2262378267
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46774059G= , CM000679.2:g.46774059G= GRCh38
NC_000017.10:g.44851425G= , CM000679.1:g.44851425G= GRCh37
NC_000017.9:g.42206588G= NCBI36
NG_008084.2:g.49658C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706495.1:c.-115-150C= (WNT3) ENSP00000516418.1:n.-115-150C=
ENST00000225512.6:c.81-150C= (WNT3) MANE Select ENSP00000225512.5:n.81-150C=
ENST00000225512.5:c.81-150C= (WNT3) ENSP00000225512.5:n.81-150C=
ENST00000573788.5:n.492-150C= (WNT3)
NM_030753.4:c.81-150C= (WNT3) NP_110380.1:n.81-150C=
XM_024450773.1:c.4809+223540G= (LRRC37A2) XP_024306541.1:n.4809+223540G=
NM_030753.5:c.81-150C= (WNT3) MANE Select NP_110380.1:n.81-150C=