Canonical Allele Identifier: CA2262384892
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46788317A= , CM000679.2:g.46788317A= GRCh38
NC_000017.10:g.44865683A= , CM000679.1:g.44865683A= GRCh37
NC_000017.9:g.42220843A= NCBI36
NG_008084.2:g.35400T=

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.-115-14408T= (WNT3) ENSP00000516418.1:n.-115-14408T=
ENST00000225512.6:c.81-14408T= (WNT3) MANE Select ENSP00000225512.5:n.81-14408T=
ENST00000225512.5:c.81-14408T= (WNT3) ENSP00000225512.5:n.81-14408T=
ENST00000573788.5:n.492-14408T= (WNT3)
NM_030753.4:c.81-14408T= (WNT3) NP_110380.1:n.81-14408T=
XM_024450773.1:c.4809+237798A= (LRRC37A2) XP_024306541.1:n.4809+237798A=
NM_030753.5:c.81-14408T= (WNT3) MANE Select NP_110380.1:n.81-14408T=
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