Canonical Allele Identifier: CA903840934

Gene: IGF2BP2

Linked Data

• dbSNP Id: rs1296695156
• MyVariant Identifiers: chr3:g.185511684_185511689del (hg19) ; chr3:g.185793896_185793901del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185793896_185793901del , CM000665.2:g.185793896_185793901del	GRCh38
NC_000003.11:g.185511684_185511689del , CM000665.1:g.185511684_185511689del	GRCh37
NC_000003.10:g.186994378_186994383del	NCBI36
NG_011602.1:g.36139_36144del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382199.7:c.239+29252_239+29257del MANE Select	ENSP00000371634.3:n.239+29252_239+29257de...
ENST00000346192.7:c.239+29252_239+29257del	ENSP00000320204.5:n.239+29252_239+29257de...
ENST00000382199.6:c.239+29252_239+29257del	ENSP00000371634.2:n.239+29252_239+29257de...
ENST00000421047.3:c.50+27111_50+27116del	ENSP00000413787.3:n.50+27111_50+27116del
ENST00000457616.6:c.239+29252_239+29257del	ENSP00000410242.2:n.239+29252_239+29257de...
ENST00000461957.5:n.119+29252_119+29257del
ENST00000466476.1:n.171+29252_171+29257del
ENST00000493302.5:n.120+27111_120+27116del
NM_001007225.1:c.239+29252_239+29257del	NP_001007226.1:n.239+29252_239+29257del
NM_001291869.1:c.239+29252_239+29257del	NP_001278798.1:n.239+29252_239+29257del
NM_001291872.1:c.50+27111_50+27116del	NP_001278801.1:n.50+27111_50+27116del
NM_001291873.1:c.50+27111_50+27116del	NP_001278802.1:n.50+27111_50+27116del
NM_001291874.1:c.50+27111_50+27116del	NP_001278803.1:n.50+27111_50+27116del
NM_001291875.1:c.-106+27111_-106+27116del	NP_001278804.1:n.-106+27111_-106+27116del...
NM_006548.4:c.239+29252_239+29257del	NP_006539.3:n.239+29252_239+29257del
XM_011512338.1:c.239+29252_239+29257del	XP_011510640.1:n.239+29252_239+29257del
XM_011512339.1:c.239+29252_239+29257del	XP_011510641.1:n.239+29252_239+29257del
XM_011512341.1:c.239+29252_239+29257del	XP_011510643.1:n.239+29252_239+29257del
XR_427358.2:n.318+29252_318+29257del
NM_001007225.2:c.239+29252_239+29257del	NP_001007226.1:n.239+29252_239+29257del
NM_001291869.2:c.239+29252_239+29257del	NP_001278798.1:n.239+29252_239+29257del
NM_001291872.2:c.50+27111_50+27116del	NP_001278801.1:n.50+27111_50+27116del
NM_001291873.2:c.50+27111_50+27116del	NP_001278802.1:n.50+27111_50+27116del
NM_001291874.2:c.50+27111_50+27116del	NP_001278803.1:n.50+27111_50+27116del
NM_001291875.2:c.-106+27111_-106+27116del	NP_001278804.1:n.-106+27111_-106+27116del...
NM_006548.5:c.239+29252_239+29257del	NP_006539.3:n.239+29252_239+29257del
NR_138486.1:n.335+29252_335+29257del
XM_017005557.2:c.178+30882_178+30887del	XP_016861046.1:n.178+30882_178+30887del
XM_017005558.2:c.239+29252_239+29257del	XP_016861047.1:n.239+29252_239+29257del
XM_017005559.2:c.239+29252_239+29257del	XP_016861048.1:n.239+29252_239+29257del
XM_017005560.2:c.35+29252_35+29257del	XP_016861049.1:n.35+29252_35+29257del
XM_017005561.1:c.239+29252_239+29257del	XP_016861050.1:n.239+29252_239+29257del
XM_017005562.1:c.239+29252_239+29257del	XP_016861051.1:n.239+29252_239+29257del
XM_017005563.1:c.239+29252_239+29257del	XP_016861052.1:n.239+29252_239+29257del
XM_017005564.1:c.239+29252_239+29257del	XP_016861053.1:n.239+29252_239+29257del
XM_024453316.1:c.-170+30882_-170+30887del	XP_024309084.1:n.-170+30882_-170+30887del...
XR_001739984.2:n.324+29252_324+29257del
NM_001007225.3:c.239+29252_239+29257del	NP_001007226.1:n.239+29252_239+29257del
NM_001291869.3:c.239+29252_239+29257del	NP_001278798.1:n.239+29252_239+29257del
NM_001291872.3:c.50+27111_50+27116del	NP_001278801.1:n.50+27111_50+27116del
NM_001291874.3:c.50+27111_50+27116del	NP_001278803.1:n.50+27111_50+27116del
NM_001291875.3:c.-106+27111_-106+27116del	NP_001278804.1:n.-106+27111_-106+27116del...
NM_006548.6:c.239+29252_239+29257del MANE Select	NP_006539.3:n.239+29252_239+29257del
NR_138486.2:n.321+29252_321+29257del
NM_001291873.3:c.50+27111_50+27116del	NP_001278802.1:n.50+27111_50+27116del