Canonical Allele Identifier: CA2638403832
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

gnomAD v4: 17-46773630-ACCCAGCCCCTCCCCCCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773633_46773649del , CM000679.2:g.46773633_46773649del GRCh38
NC_000017.10:g.44850999_44851015del , CM000679.1:g.44850999_44851015del GRCh37
NC_000017.9:g.42206162_42206178del NCBI36
NG_008084.2:g.50070_50086del

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+21_127+37del (WNT3) ENSP00000516418.1:n.127+21_127+37del
ENST00000225512.6:c.322+21_322+37del (WNT3) MANE Select ENSP00000225512.5:n.322+21_322+37del
ENST00000225512.5:c.322+21_322+37del (WNT3) ENSP00000225512.5:n.322+21_322+37del
NM_030753.4:c.322+21_322+37del (WNT3) NP_110380.1:n.322+21_322+37del
XM_024450773.1:c.4809+223114_4809+223130del (LRRC37A2) XP_024306541.1:n.4809+223114_4809+223130d...
NM_030753.5:c.322+21_322+37del (WNT3) MANE Select NP_110380.1:n.322+21_322+37del
Search 100 bp 5'
Search 100 bp 3'