Canonical Allele Identifier: CA626684291
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs368579618
gnomAD v2: 17-44851006-T-TCC
gnomAD v3: 17-46773640-T-TCC
gnomAD v4: 17-46773640-T-TCC
MyVariant Identifiers: chr17:g.44851007_44851008insCC (hg19) chr17:g.44851006_44851007insCC (hg19) chr17:g.46773641_46773642insCC (hg38) chr17:g.46773640_46773641insCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773648_46773649dup , CM000679.2:g.46773648_46773649dup GRCh38
NC_000017.10:g.44851014_44851015dup , CM000679.1:g.44851014_44851015dup GRCh37
NC_000017.9:g.42206177_42206178dup NCBI36
NG_008084.2:g.50075_50076dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+26_127+27dup (WNT3) ENSP00000516418.1:n.127+26_127+27dup
ENST00000225512.6:c.322+26_322+27dup (WNT3) MANE Select ENSP00000225512.5:n.322+26_322+27dup
ENST00000225512.5:c.322+26_322+27dup (WNT3) ENSP00000225512.5:n.322+26_322+27dup
NM_030753.4:c.322+26_322+27dup (WNT3) NP_110380.1:n.322+26_322+27dup
XM_024450773.1:c.4809+223129_4809+223130dup (LRRC37A2) XP_024306541.1:n.4809+223129_4809+223130d...
NM_030753.5:c.322+26_322+27dup (WNT3) MANE Select NP_110380.1:n.322+26_322+27dup
Search 100 bp 5'
Search 100 bp 3'