Canonical Allele Identifier: CA2580615594

Gene: INS INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2160002_2160003insGCGCAGTGGCAGGTGCCCCACTGCGC , CM000673.2:g.2160002_2160003insGCGCAGTGGCAGGTGCCCCACTGCGC	GRCh38
NC_000011.9:g.2181232_2181233insGCGCAGTGGCAGGTGCCCCACTGCGC , CM000673.1:g.2181232_2181233insGCGCAGTGGCAGGTGCCCCACTGCGC	GRCh37
NC_000011.8:g.2137808_2137809insGCGCAGTGGCAGGTGCCCCACTGCGC	NCBI36
NG_007114.1:g.6193_6194insCGCAGTGGGGCACCTGCCACTGCGCG
NG_050578.1:g.6208_6209insCGCAGTGGGGCACCTGCCACTGCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381330.5:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS) MANE Select	ENSP00000370731.5:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
ENST00000250971.7:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	ENSP00000250971.3:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
ENST00000356578.8:c.187+783_187+784insCGCAGTGGGGCACCTGCCACTGCGCG (INS-IGF2)	ENSP00000348986.4:n.187+783_187+784insCGCAGTGGGGCACCTGCCACTGC...
ENST00000381330.4:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	ENSP00000370731.4:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
ENST00000397262.5:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	ENSP00000380432.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
ENST00000397270.1:c.187+783_187+784insCGCAGTGGGGCACCTGCCACTGCGCG (INS-IGF2)	ENSP00000380440.1:n.187+783_187+784insCGCAGTGGGGCACCTGCCACTGC...
ENST00000421783.1:c.188-130_188-129insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	ENSP00000408400.1:n.188-130_188-129insCGCAGTGGGGCACCTGCCACTGC...
ENST00000512523.1:c.188-41_188-40insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	ENSP00000424008.1:n.188-41_188-40insCGCAGTGGGGCACCTGCCACTGCGC...
NM_000207.2:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_000198.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NM_001042376.2:c.187+783_187+784insCGCAGTGGGGCACCTGCCACTGCGCG (INS-IGF2)	NP_001035835.1:n.187+783_187+784insCGCAGTGGGGCACCTGCCACTGCGCG...
NM_001185097.1:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_001172026.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NM_001185098.1:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_001172027.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NM_001291897.1:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_001278826.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NR_003512.3:n.246+783_246+784insCGCAGTGGGGCACCTGCCACTGCGCG (INS-IGF2)
NM_000207.3:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS) MANE Select	NP_000198.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NM_001042376.3:c.187+783_187+784insCGCAGTGGGGCACCTGCCACTGCGCG (INS-IGF2)	NP_001035835.1:n.187+783_187+784insCGCAGTGGGGCACCTGCCACTGCGCG...
NM_001185097.2:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_001172026.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NM_001291897.2:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_001278826.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG
NR_003512.4:n.246+783_246+784insCGCAGTGGGGCACCTGCCACTGCGCG (INS-IGF2)
NM_001185098.2:c.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG (INS)	NP_001172027.1:n.188-5_188-4insCGCAGTGGGGCACCTGCCACTGCGCG