Canonical Allele Identifier: CA918805008

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs1590146629
• gnomAD v4: 11-2149364-CTTTTAGAGTGTGCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149365_2149379del , CM000673.2:g.2149365_2149379del	GRCh38
NC_000011.9:g.2170595_2170609del , CM000673.1:g.2170595_2170609del	GRCh37
NC_000011.8:g.2127171_2127185del	NCBI36
NG_008849.1:g.5225_5239del
NG_050578.1:g.16831_16845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-468-34_-468-20del (IGF2)	ENSP00000511998.1:n.-468-34_-468-20del
ENST00000643349.2:c.1_15del	ENSP00000495715.1:p.Met1_Lys5del
ENST00000695541.1:c.-468-34_-468-20del (IGF2)	ENSP00000511997.1:n.-468-34_-468-20del
ENST00000481781.2:n.126-34_126-20del
ENST00000643349.1:c.1_15del	ENSP00000495715.1:p.Met1_Lys5del
ENST00000356578.8:c.188-34_188-20del (INS-IGF2)	ENSP00000348986.4:n.188-34_188-20del
ENST00000397270.1:c.188-34_188-20del (INS-IGF2)	ENSP00000380440.1:n.188-34_188-20del
ENST00000476874.1:n.71-34_71-20del (INS-IGF2)
ENST00000481781.1:n.393-34_393-20del (INS-IGF2)
NM_001007139.5:c.-502_-488del (IGF2)	NP_001007140.2:n.-502_-488del
NM_001042376.2:c.188-34_188-20del (INS-IGF2)	NP_001035835.1:n.188-34_188-20del
NR_003512.3:n.247-34_247-20del (INS-IGF2)
NM_001042376.3:c.188-34_188-20del (INS-IGF2)	NP_001035835.1:n.188-34_188-20del
NR_003512.4:n.247-34_247-20del (INS-IGF2)
NM_001007139.6:c.-502_-488del (IGF2)	NP_001007140.2:n.-502_-488del