Canonical Allele Identifier: CA379114122

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2135531T>C , CM000673.2:g.2135531T>C	GRCh38
NC_000011.9:g.2156761T>C , CM000673.1:g.2156761T>C	GRCh37
NC_000011.8:g.2113337T>C	NCBI36
NG_008849.1:g.19073A>G
NG_050578.1:g.30679A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000612.6:c.-6-2A>G (IGF2) MANE Select	NP_000603.1:n.-6-2A>G
ENST00000416167.7:c.-6-2A>G (IGF2) MANE Select	ENSP00000414497.2:n.-6-2A>G
NM_000612.5:c.-6-2A>G (IGF2)	NP_000603.1:n.-6-2A>G
NM_001007139.5:c.-6-2A>G (IGF2)	NP_001007140.2:n.-6-2A>G
NM_001007139.6:c.-6-2A>G (IGF2)	NP_001007140.2:n.-6-2A>G
NM_001127598.2:c.163-2A>G (IGF2)	NP_001121070.1:n.163-2A>G
NM_001127598.3:c.163-2A>G (IGF2)	NP_001121070.1:n.163-2A>G
NM_001291861.2:c.-6-2A>G (IGF2)	NP_001278790.1:n.-6-2A>G
NM_001291861.3:c.-6-2A>G (IGF2)	NP_001278790.1:n.-6-2A>G
NM_001291862.2:c.-6-2A>G (IGF2)	NP_001278791.1:n.-6-2A>G
NM_001291862.3:c.-6-2A>G (IGF2)	NP_001278791.1:n.-6-2A>G
NR_003512.3:n.709-2A>G (INS-IGF2)
NR_003512.4:n.709-2A>G (INS-IGF2)
ENST00000356578.8:c.*47-2A>G (INS-IGF2)	ENSP00000348986.4:n.*47-2A>G
ENST00000381389.5:c.-6-2A>G (IGF2)	ENSP00000370796.1:n.-6-2A>G
ENST00000381392.5:c.-6-2A>G (IGF2)	ENSP00000370799.1:n.-6-2A>G
ENST00000381395.5:c.-6-2A>G (IGF2)	ENSP00000370802.1:n.-6-2A>G
ENST00000381406.8:c.-6-2A>G (IGF2)	ENSP00000370813.4:n.-6-2A>G
ENST00000416167.6:c.-6-2A>G (IGF2)	ENSP00000414497.2:n.-6-2A>G
ENST00000418738.2:c.-6-2A>G (IGF2)	ENSP00000402047.2:n.-6-2A>G
ENST00000434045.6:c.163-2A>G (IGF2)	ENSP00000391826.2:n.163-2A>G
ENST00000481781.3:c.-6-2A>G (IGF2)	ENSP00000511998.1:n.-6-2A>G
ENST00000643349.1:c.*47-2A>G	ENSP00000495715.1:n.*47-2A>G
ENST00000643349.2:c.*47-2A>G	ENSP00000495715.1:n.*47-2A>G
ENST00000695541.1:c.-6-2A>G (IGF2)	ENSP00000511997.1:n.-6-2A>G