Canonical Allele Identifier: CA16042778
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 372980
ClinVar RCV Id: RCV000414320
dbSNP Id: rs1057518115

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2135427A>G , CM000673.2:g.2135427A>G GRCh38
NC_000011.9:g.2156657A>G , CM000673.1:g.2156657A>G GRCh37
NC_000011.8:g.2113233A>G NCBI36
NG_008849.1:g.19177T>C
NG_050578.1:g.30783T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000481781.3:c.97T>C (IGF2) ENSP00000511998.1:p.Cys33Arg
ENST00000643349.2:c.*149T>C ENSP00000495715.1:n.*149T>C
ENST00000695541.1:c.97T>C (IGF2) ENSP00000511997.1:p.Cys33Arg
ENST00000416167.7:c.97T>C (IGF2) MANE Select ENSP00000414497.2:p.Cys33Arg
ENST00000643349.1:c.*149T>C ENSP00000495715.1:n.*149T>C
ENST00000356578.8:c.*149T>C (INS-IGF2) ENSP00000348986.4:n.*149T>C
ENST00000381389.5:c.97T>C (IGF2) ENSP00000370796.1:p.Cys33Arg
ENST00000381392.5:c.97T>C (IGF2) ENSP00000370799.1:p.Cys33Arg
ENST00000381395.5:c.97T>C (IGF2) ENSP00000370802.1:p.Cys33Arg
ENST00000381406.8:c.97T>C (IGF2) ENSP00000370813.4:p.Cys33Arg
ENST00000416167.6:c.97T>C (IGF2) ENSP00000414497.2:p.Cys33Arg
ENST00000418738.2:c.97T>C (IGF2) ENSP00000402047.2:p.Cys33Arg
ENST00000434045.6:c.265T>C (IGF2) ENSP00000391826.2:p.Cys89Arg
NM_000612.5:c.97T>C (IGF2) NP_000603.1:p.Cys33Arg
NM_001007139.5:c.97T>C (IGF2) NP_001007140.2:p.Cys33Arg
NM_001127598.2:c.265T>C (IGF2) NP_001121070.1:p.Cys89Arg
NM_001291861.2:c.97T>C (IGF2) NP_001278790.1:p.Cys33Arg
NM_001291862.2:c.97T>C (IGF2) NP_001278791.1:p.Cys33Arg
NR_003512.3:n.811T>C (INS-IGF2)
NM_000612.6:c.97T>C (IGF2) MANE Select NP_000603.1:p.Cys33Arg
NM_001127598.3:c.265T>C (IGF2) NP_001121070.1:p.Cys89Arg
NM_001291861.3:c.97T>C (IGF2) NP_001278790.1:p.Cys33Arg
NM_001291862.3:c.97T>C (IGF2) NP_001278791.1:p.Cys33Arg
NR_003512.4:n.811T>C (INS-IGF2)
NM_001007139.6:c.97T>C (IGF2) NP_001007140.2:p.Cys33Arg