Canonical Allele Identifier: CA2531061052

Gene: IGF2BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185811464_185811465del , CM000665.2:g.185811464_185811465del	GRCh38
NC_000003.11:g.185529252_185529253del , CM000665.1:g.185529252_185529253del	GRCh37
NC_000003.10:g.187011946_187011947del	NCBI36
NG_011602.1:g.18576_18577del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382199.7:c.239+11689_239+11690del MANE Select	ENSP00000371634.3:n.239+11689_239+11690de...
ENST00000346192.7:c.239+11689_239+11690del	ENSP00000320204.5:n.239+11689_239+11690de...
ENST00000382199.6:c.239+11689_239+11690del	ENSP00000371634.2:n.239+11689_239+11690de...
ENST00000421047.3:c.50+9548_50+9549del	ENSP00000413787.3:n.50+9548_50+9549del
ENST00000457616.6:c.239+11689_239+11690del	ENSP00000410242.2:n.239+11689_239+11690de...
ENST00000461957.5:n.119+11689_119+11690del
ENST00000466476.1:n.171+11689_171+11690del
ENST00000493302.5:n.120+9548_120+9549del
NM_001007225.1:c.239+11689_239+11690del	NP_001007226.1:n.239+11689_239+11690del
NM_001291869.1:c.239+11689_239+11690del	NP_001278798.1:n.239+11689_239+11690del
NM_001291872.1:c.50+9548_50+9549del	NP_001278801.1:n.50+9548_50+9549del
NM_001291873.1:c.50+9548_50+9549del	NP_001278802.1:n.50+9548_50+9549del
NM_001291874.1:c.50+9548_50+9549del	NP_001278803.1:n.50+9548_50+9549del
NM_001291875.1:c.-106+9548_-106+9549del	NP_001278804.1:n.-106+9548_-106+9549del
NM_006548.4:c.239+11689_239+11690del	NP_006539.3:n.239+11689_239+11690del
XM_011512338.1:c.239+11689_239+11690del	XP_011510640.1:n.239+11689_239+11690del
XM_011512339.1:c.239+11689_239+11690del	XP_011510641.1:n.239+11689_239+11690del
XM_011512341.1:c.239+11689_239+11690del	XP_011510643.1:n.239+11689_239+11690del
XR_427358.2:n.318+11689_318+11690del
NM_001007225.2:c.239+11689_239+11690del	NP_001007226.1:n.239+11689_239+11690del
NM_001291869.2:c.239+11689_239+11690del	NP_001278798.1:n.239+11689_239+11690del
NM_001291872.2:c.50+9548_50+9549del	NP_001278801.1:n.50+9548_50+9549del
NM_001291873.2:c.50+9548_50+9549del	NP_001278802.1:n.50+9548_50+9549del
NM_001291874.2:c.50+9548_50+9549del	NP_001278803.1:n.50+9548_50+9549del
NM_001291875.2:c.-106+9548_-106+9549del	NP_001278804.1:n.-106+9548_-106+9549del
NM_006548.5:c.239+11689_239+11690del	NP_006539.3:n.239+11689_239+11690del
NR_138486.1:n.335+11689_335+11690del
XM_017005557.2:c.178+13319_178+13320del	XP_016861046.1:n.178+13319_178+13320del
XM_017005558.2:c.239+11689_239+11690del	XP_016861047.1:n.239+11689_239+11690del
XM_017005559.2:c.239+11689_239+11690del	XP_016861048.1:n.239+11689_239+11690del
XM_017005560.2:c.35+11689_35+11690del	XP_016861049.1:n.35+11689_35+11690del
XM_017005561.1:c.239+11689_239+11690del	XP_016861050.1:n.239+11689_239+11690del
XM_017005562.1:c.239+11689_239+11690del	XP_016861051.1:n.239+11689_239+11690del
XM_017005563.1:c.239+11689_239+11690del	XP_016861052.1:n.239+11689_239+11690del
XM_017005564.1:c.239+11689_239+11690del	XP_016861053.1:n.239+11689_239+11690del
XM_024453316.1:c.-170+13319_-170+13320del	XP_024309084.1:n.-170+13319_-170+13320del...
XR_001739984.2:n.324+11689_324+11690del
NM_001007225.3:c.239+11689_239+11690del	NP_001007226.1:n.239+11689_239+11690del
NM_001291869.3:c.239+11689_239+11690del	NP_001278798.1:n.239+11689_239+11690del
NM_001291872.3:c.50+9548_50+9549del	NP_001278801.1:n.50+9548_50+9549del
NM_001291874.3:c.50+9548_50+9549del	NP_001278803.1:n.50+9548_50+9549del
NM_001291875.3:c.-106+9548_-106+9549del	NP_001278804.1:n.-106+9548_-106+9549del
NM_006548.6:c.239+11689_239+11690del MANE Select	NP_006539.3:n.239+11689_239+11690del
NR_138486.2:n.321+11689_321+11690del
NM_001291873.3:c.50+9548_50+9549del	NP_001278802.1:n.50+9548_50+9549del