Canonical Allele Identifier: CA379113301

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2133173C>T , CM000673.2:g.2133173C>T	GRCh38
NC_000011.9:g.2154403C>T , CM000673.1:g.2154403C>T	GRCh37
NC_000011.8:g.2110979C>T	NCBI36
NG_008849.1:g.21431G>A
NG_050578.1:g.33037G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.357G>A (IGF2)	ENSP00000511998.1:p.Trp119Ter
ENST00000643349.2:c.*409G>A	ENSP00000495715.1:n.*409G>A
ENST00000695541.1:c.357G>A (IGF2)	ENSP00000511997.1:p.Trp119Ter
ENST00000416167.7:c.357G>A (IGF2) MANE Select	ENSP00000414497.2:p.Trp119Ter
ENST00000643349.1:c.*409G>A	ENSP00000495715.1:n.*409G>A
ENST00000356578.8:c.*409G>A (INS-IGF2)	ENSP00000348986.4:n.*409G>A
ENST00000381389.5:c.357G>A (IGF2)	ENSP00000370796.1:p.Trp119Ter
ENST00000381392.5:c.366G>A (IGF2)	ENSP00000370799.1:p.Trp122Ter
ENST00000381395.5:c.357G>A (IGF2)	ENSP00000370802.1:p.Trp119Ter
ENST00000381406.8:c.366G>A (IGF2)	ENSP00000370813.4:p.Trp122Ter
ENST00000416167.6:c.357G>A (IGF2)	ENSP00000414497.2:p.Trp119Ter
ENST00000418738.2:c.357G>A (IGF2)	ENSP00000402047.2:p.Trp119Ter
ENST00000434045.6:c.525G>A (IGF2)	ENSP00000391826.2:p.Trp175Ter
NM_000612.5:c.357G>A (IGF2)	NP_000603.1:p.Trp119Ter
NM_001007139.5:c.357G>A (IGF2)	NP_001007140.2:p.Trp119Ter
NM_001127598.2:c.525G>A (IGF2)	NP_001121070.1:p.Trp175Ter
NM_001291861.2:c.357G>A (IGF2)	NP_001278790.1:p.Trp119Ter
NM_001291862.2:c.357G>A (IGF2)	NP_001278791.1:p.Trp119Ter
NR_003512.3:n.1071G>A (INS-IGF2)
NM_000612.6:c.357G>A (IGF2) MANE Select	NP_000603.1:p.Trp119Ter
NM_001127598.3:c.525G>A (IGF2)	NP_001121070.1:p.Trp175Ter
NM_001291861.3:c.357G>A (IGF2)	NP_001278790.1:p.Trp119Ter
NM_001291862.3:c.357G>A (IGF2)	NP_001278791.1:p.Trp119Ter
NR_003512.4:n.1071G>A (INS-IGF2)
NM_001007139.6:c.357G>A (IGF2)	NP_001007140.2:p.Trp119Ter