Canonical Allele Identifier: CA2638403745
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773630_46773649del , CM000679.2:g.46773630_46773649del GRCh38
NC_000017.10:g.44850996_44851015del , CM000679.1:g.44850996_44851015del GRCh37
NC_000017.9:g.42206159_42206178del NCBI36
NG_008084.2:g.50074_50093del

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+25_127+44del (WNT3) ENSP00000516418.1:n.127+25_127+44del
ENST00000225512.6:c.322+25_322+44del (WNT3) MANE Select ENSP00000225512.5:n.322+25_322+44del
ENST00000225512.5:c.322+25_322+44del (WNT3) ENSP00000225512.5:n.322+25_322+44del
NM_030753.4:c.322+25_322+44del (WNT3) NP_110380.1:n.322+25_322+44del
XM_024450773.1:c.4809+223111_4809+223130del (LRRC37A2) XP_024306541.1:n.4809+223111_4809+223130d...
NM_030753.5:c.322+25_322+44del (WNT3) MANE Select NP_110380.1:n.322+25_322+44del