Canonical Allele Identifier: CA1057337922

Gene: IGF2BP2

Linked Data

• gnomAD v3: 3-185794301-TCAC-T
• gnomAD v4: 3-185794301-TCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185794302_185794304del , CM000665.2:g.185794302_185794304del	GRCh38
NC_000003.11:g.185512090_185512092del , CM000665.1:g.185512090_185512092del	GRCh37
NC_000003.10:g.186994784_186994786del	NCBI36
NG_011602.1:g.35736_35738del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382199.7:c.239+28849_239+28851del MANE Select	ENSP00000371634.3:n.239+28849_239+28851del
ENST00000346192.7:c.239+28849_239+28851del	ENSP00000320204.5:n.239+28849_239+28851del
ENST00000382199.6:c.239+28849_239+28851del	ENSP00000371634.2:n.239+28849_239+28851del
ENST00000421047.3:c.50+26708_50+26710del	ENSP00000413787.3:n.50+26708_50+26710del
ENST00000457616.6:c.239+28849_239+28851del	ENSP00000410242.2:n.239+28849_239+28851del
ENST00000461957.5:n.119+28849_119+28851del
ENST00000466476.1:n.171+28849_171+28851del
ENST00000493302.5:n.120+26708_120+26710del
NM_001007225.1:c.239+28849_239+28851del	NP_001007226.1:n.239+28849_239+28851del
NM_001291869.1:c.239+28849_239+28851del	NP_001278798.1:n.239+28849_239+28851del
NM_001291872.1:c.50+26708_50+26710del	NP_001278801.1:n.50+26708_50+26710del
NM_001291873.1:c.50+26708_50+26710del	NP_001278802.1:n.50+26708_50+26710del
NM_001291874.1:c.50+26708_50+26710del	NP_001278803.1:n.50+26708_50+26710del
NM_001291875.1:c.-106+26708_-106+26710del	NP_001278804.1:n.-106+26708_-106+26710del
NM_006548.4:c.239+28849_239+28851del	NP_006539.3:n.239+28849_239+28851del
XM_011512338.1:c.239+28849_239+28851del	XP_011510640.1:n.239+28849_239+28851del
XM_011512339.1:c.239+28849_239+28851del	XP_011510641.1:n.239+28849_239+28851del
XM_011512341.1:c.239+28849_239+28851del	XP_011510643.1:n.239+28849_239+28851del
XR_427358.2:n.318+28849_318+28851del
NM_001007225.2:c.239+28849_239+28851del	NP_001007226.1:n.239+28849_239+28851del
NM_001291869.2:c.239+28849_239+28851del	NP_001278798.1:n.239+28849_239+28851del
NM_001291872.2:c.50+26708_50+26710del	NP_001278801.1:n.50+26708_50+26710del
NM_001291873.2:c.50+26708_50+26710del	NP_001278802.1:n.50+26708_50+26710del
NM_001291874.2:c.50+26708_50+26710del	NP_001278803.1:n.50+26708_50+26710del
NM_001291875.2:c.-106+26708_-106+26710del	NP_001278804.1:n.-106+26708_-106+26710del
NM_006548.5:c.239+28849_239+28851del	NP_006539.3:n.239+28849_239+28851del
NR_138486.1:n.335+28849_335+28851del
XM_017005557.2:c.178+30479_178+30481del	XP_016861046.1:n.178+30479_178+30481del
XM_017005558.2:c.239+28849_239+28851del	XP_016861047.1:n.239+28849_239+28851del
XM_017005559.2:c.239+28849_239+28851del	XP_016861048.1:n.239+28849_239+28851del
XM_017005560.2:c.35+28849_35+28851del	XP_016861049.1:n.35+28849_35+28851del
XM_017005561.1:c.239+28849_239+28851del	XP_016861050.1:n.239+28849_239+28851del
XM_017005562.1:c.239+28849_239+28851del	XP_016861051.1:n.239+28849_239+28851del
XM_017005563.1:c.239+28849_239+28851del	XP_016861052.1:n.239+28849_239+28851del
XM_017005564.1:c.239+28849_239+28851del	XP_016861053.1:n.239+28849_239+28851del
XM_024453316.1:c.-170+30479_-170+30481del	XP_024309084.1:n.-170+30479_-170+30481del
XR_001739984.2:n.324+28849_324+28851del
NM_001007225.3:c.239+28849_239+28851del	NP_001007226.1:n.239+28849_239+28851del
NM_001291869.3:c.239+28849_239+28851del	NP_001278798.1:n.239+28849_239+28851del
NM_001291872.3:c.50+26708_50+26710del	NP_001278801.1:n.50+26708_50+26710del
NM_001291874.3:c.50+26708_50+26710del	NP_001278803.1:n.50+26708_50+26710del
NM_001291875.3:c.-106+26708_-106+26710del	NP_001278804.1:n.-106+26708_-106+26710del
NM_006548.6:c.239+28849_239+28851del MANE Select	NP_006539.3:n.239+28849_239+28851del
NR_138486.2:n.321+28849_321+28851del
NM_001291873.3:c.50+26708_50+26710del	NP_001278802.1:n.50+26708_50+26710del