Canonical Allele Identifier: CA8620625
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs368579618
ExAC: 17:44851006 TC / T
gnomAD v2: 17-44851006-TC-T
gnomAD v3: 17-46773640-TC-T
gnomAD v4: 17-46773640-TC-T
COSMIC: COSN20065812
MyVariant Identifiers: chr17:g.44851008del (hg19) chr17:g.44851007del (hg19) chr17:g.46773641del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773649del , CM000679.2:g.46773649del GRCh38
NC_000017.10:g.44851015del , CM000679.1:g.44851015del GRCh37
NC_000017.9:g.42206178del NCBI36
NG_008084.2:g.50076del

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+27del (WNT3) ENSP00000516418.1:n.127+27del
ENST00000225512.6:c.322+27del (WNT3) MANE Select ENSP00000225512.5:n.322+27del
ENST00000225512.5:c.322+27del (WNT3) ENSP00000225512.5:n.322+27del
NM_030753.4:c.322+27del (WNT3) NP_110380.1:n.322+27del
XM_024450773.1:c.4809+223130del (LRRC37A2) XP_024306541.1:n.4809+223130del
NM_030753.5:c.322+27del (WNT3) MANE Select NP_110380.1:n.322+27del
Search 100 bp 5'
Search 100 bp 3'