Canonical Allele Identifier: CA772509589
Gene: WNT3 HGNC NCBI
LRRC37A2 HGNC NCBI

Linked Data

dbSNP Id: rs1271175569
MyVariant Identifiers: chr17:g.44851010_44851011insG (hg19) chr17:g.46773644_46773645insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46773644_46773645insG , CM000679.2:g.46773644_46773645insG GRCh38
NC_000017.10:g.44851010_44851011insG , CM000679.1:g.44851010_44851011insG GRCh37
NC_000017.9:g.42206173_42206174insG NCBI36
NG_008084.2:g.50072_50073insC

Transcript Alleles

HGVS Amino-acid change
ENST00000706495.1:c.127+23_127+24insC (WNT3) ENSP00000516418.1:n.127+23_127+24insC
ENST00000225512.6:c.322+23_322+24insC (WNT3) MANE Select ENSP00000225512.5:n.322+23_322+24insC
ENST00000225512.5:c.322+23_322+24insC (WNT3) ENSP00000225512.5:n.322+23_322+24insC
NM_030753.4:c.322+23_322+24insC (WNT3) NP_110380.1:n.322+23_322+24insC
XM_024450773.1:c.4809+223125_4809+223126insG (LRRC37A2) XP_024306541.1:n.4809+223125_4809+223126i...
NM_030753.5:c.322+23_322+24insC (WNT3) MANE Select NP_110380.1:n.322+23_322+24insC
Search 100 bp 5'
Search 100 bp 3'