Canonical Allele Identifier: CA1426641961

Gene: IGF2BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185793974_185793977delinsTTTG , CM000665.2:g.185793974_185793977delinsTTTG	GRCh38
NC_000003.11:g.185511762_185511765delinsTTTG , CM000665.1:g.185511762_185511765delinsTTTG	GRCh37
NC_000003.10:g.186994456_186994459delinsTTTG	NCBI36
NG_011602.1:g.36063_36066delinsCAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000382199.7:c.239+29176_239+29179delinsCAAA MANE Select	ENSP00000371634.3:n.239+29176_239+29179de...
ENST00000346192.7:c.239+29176_239+29179delinsCAAA	ENSP00000320204.5:n.239+29176_239+29179de...
ENST00000382199.6:c.239+29176_239+29179delinsCAAA	ENSP00000371634.2:n.239+29176_239+29179de...
ENST00000421047.3:c.50+27035_50+27038delinsCAAA	ENSP00000413787.3:n.50+27035_50+27038deli...
ENST00000457616.6:c.239+29176_239+29179delinsCAAA	ENSP00000410242.2:n.239+29176_239+29179de...
ENST00000461957.5:n.119+29176_119+29179delinsCAAA
ENST00000466476.1:n.171+29176_171+29179delinsCAAA
ENST00000493302.5:n.120+27035_120+27038delinsCAAA
NM_001007225.1:c.239+29176_239+29179delinsCAAA	NP_001007226.1:n.239+29176_239+29179delin...
NM_001291869.1:c.239+29176_239+29179delinsCAAA	NP_001278798.1:n.239+29176_239+29179delin...
NM_001291872.1:c.50+27035_50+27038delinsCAAA	NP_001278801.1:n.50+27035_50+27038delinsC...
NM_001291873.1:c.50+27035_50+27038delinsCAAA	NP_001278802.1:n.50+27035_50+27038delinsC...
NM_001291874.1:c.50+27035_50+27038delinsCAAA	NP_001278803.1:n.50+27035_50+27038delinsC...
NM_001291875.1:c.-106+27035_-106+27038delinsCAAA	NP_001278804.1:n.-106+27035_-106+27038del...
NM_006548.4:c.239+29176_239+29179delinsCAAA	NP_006539.3:n.239+29176_239+29179delinsCA...
XM_011512338.1:c.239+29176_239+29179delinsCAAA	XP_011510640.1:n.239+29176_239+29179delin...
XM_011512339.1:c.239+29176_239+29179delinsCAAA	XP_011510641.1:n.239+29176_239+29179delin...
XM_011512341.1:c.239+29176_239+29179delinsCAAA	XP_011510643.1:n.239+29176_239+29179delin...
XR_427358.2:n.318+29176_318+29179delinsCAAA
NM_001007225.2:c.239+29176_239+29179delinsCAAA	NP_001007226.1:n.239+29176_239+29179delin...
NM_001291869.2:c.239+29176_239+29179delinsCAAA	NP_001278798.1:n.239+29176_239+29179delin...
NM_001291872.2:c.50+27035_50+27038delinsCAAA	NP_001278801.1:n.50+27035_50+27038delinsC...
NM_001291873.2:c.50+27035_50+27038delinsCAAA	NP_001278802.1:n.50+27035_50+27038delinsC...
NM_001291874.2:c.50+27035_50+27038delinsCAAA	NP_001278803.1:n.50+27035_50+27038delinsC...
NM_001291875.2:c.-106+27035_-106+27038delinsCAAA	NP_001278804.1:n.-106+27035_-106+27038del...
NM_006548.5:c.239+29176_239+29179delinsCAAA	NP_006539.3:n.239+29176_239+29179delinsCA...
NR_138486.1:n.335+29176_335+29179delinsCAAA
XM_017005557.2:c.178+30806_178+30809delinsCAAA	XP_016861046.1:n.178+30806_178+30809delin...
XM_017005558.2:c.239+29176_239+29179delinsCAAA	XP_016861047.1:n.239+29176_239+29179delin...
XM_017005559.2:c.239+29176_239+29179delinsCAAA	XP_016861048.1:n.239+29176_239+29179delin...
XM_017005560.2:c.35+29176_35+29179delinsCAAA	XP_016861049.1:n.35+29176_35+29179delinsC...
XM_017005561.1:c.239+29176_239+29179delinsCAAA	XP_016861050.1:n.239+29176_239+29179delin...
XM_017005562.1:c.239+29176_239+29179delinsCAAA	XP_016861051.1:n.239+29176_239+29179delin...
XM_017005563.1:c.239+29176_239+29179delinsCAAA	XP_016861052.1:n.239+29176_239+29179delin...
XM_017005564.1:c.239+29176_239+29179delinsCAAA	XP_016861053.1:n.239+29176_239+29179delin...
XM_024453316.1:c.-170+30806_-170+30809delinsCAAA	XP_024309084.1:n.-170+30806_-170+30809del...
XR_001739984.2:n.324+29176_324+29179delinsCAAA
NM_001007225.3:c.239+29176_239+29179delinsCAAA	NP_001007226.1:n.239+29176_239+29179delin...
NM_001291869.3:c.239+29176_239+29179delinsCAAA	NP_001278798.1:n.239+29176_239+29179delin...
NM_001291872.3:c.50+27035_50+27038delinsCAAA	NP_001278801.1:n.50+27035_50+27038delinsC...
NM_001291874.3:c.50+27035_50+27038delinsCAAA	NP_001278803.1:n.50+27035_50+27038delinsC...
NM_001291875.3:c.-106+27035_-106+27038delinsCAAA	NP_001278804.1:n.-106+27035_-106+27038del...
NM_006548.6:c.239+29176_239+29179delinsCAAA MANE Select	NP_006539.3:n.239+29176_239+29179delinsCA...
NR_138486.2:n.321+29176_321+29179delinsCAAA
NM_001291873.3:c.50+27035_50+27038delinsCAAA	NP_001278802.1:n.50+27035_50+27038delinsC...