Canonical Allele Identifier: CA2638403901
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773640_46773643del , CM000679.2:g.46773640_46773643del GRCh38
NC_000017.10:g.44851006_44851009del , CM000679.1:g.44851006_44851009del GRCh37
NC_000017.9:g.42206169_42206172del NCBI36
NG_008084.2:g.50077_50080del

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+28_127+31del (WNT3) ENSP00000516418.1:n.127+28_127+31del
ENST00000225512.6:c.322+28_322+31del (WNT3) MANE Select ENSP00000225512.5:n.322+28_322+31del
ENST00000225512.5:c.322+28_322+31del (WNT3) ENSP00000225512.5:n.322+28_322+31del
NM_030753.4:c.322+28_322+31del (WNT3) NP_110380.1:n.322+28_322+31del
XM_024450773.1:c.4809+223121_4809+223124del (LRRC37A2) XP_024306541.1:n.4809+223121_4809+223124d...
NM_030753.5:c.322+28_322+31del (WNT3) MANE Select NP_110380.1:n.322+28_322+31del