Canonical Allele Identifier: CA626684280
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs2059391964
gnomAD v2: 17-44850998-C-CCAGCCCCTCCCCCCCCCT
gnomAD v3: 17-46773632-C-CCAGCCCCTCCCCCCCCCT
gnomAD v4: 17-46773632-C-CCAGCCCCTCCCCCCCCCT
MyVariant Identifiers: chr17:g.44850998_44850999insCAGCCCCTCCCCCCCCCT (hg19) chr17:g.46773632_46773633insCAGCCCCTCCCCCCCCCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773640_46773657dup , CM000679.2:g.46773640_46773657dup GRCh38
NC_000017.10:g.44851006_44851023dup , CM000679.1:g.44851006_44851023dup GRCh37
NC_000017.9:g.42206169_42206186dup NCBI36
NG_008084.2:g.50067_50084dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+18_127+35dup (WNT3) ENSP00000516418.1:n.127+18_127+35dup
ENST00000225512.6:c.322+18_322+35dup (WNT3) MANE Select ENSP00000225512.5:n.322+18_322+35dup
ENST00000225512.5:c.322+18_322+35dup (WNT3) ENSP00000225512.5:n.322+18_322+35dup
NM_030753.4:c.322+18_322+35dup (WNT3) NP_110380.1:n.322+18_322+35dup
XM_024450773.1:c.4809+223121_4809+223138dup (LRRC37A2) XP_024306541.1:n.4809+223121_4809+223138d...
NM_030753.5:c.322+18_322+35dup (WNT3) MANE Select NP_110380.1:n.322+18_322+35dup
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