Canonical Allele Identifier: CA645369514

Gene: IGF2 INS-IGF2

Linked Data

• ClinVar Variation Id: 253298
• ClinVar RCV Id: RCV000490875
• dbSNP Id: rs1114167321
• MyVariant Identifiers: chr11:g.2156596_2156597insGC (hg19) ; chr11:g.2135366_2135367insGC (hg38)
• PubMed: PMID:28796236

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2135366_2135367insGC , CM000673.2:g.2135366_2135367insGC	GRCh38
NC_000011.9:g.2156596_2156597insGC , CM000673.1:g.2156596_2156597insGC	GRCh37
NC_000011.8:g.2113172_2113173insGC	NCBI36
NG_008849.1:g.19238_19239insCG
NG_050578.1:g.30844_30845insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.157+1_157+2insCG (IGF2)	ENSP00000511998.1:n.157+1_157+2insCG
ENST00000643349.2:c.*209+1_*209+2insCG	ENSP00000495715.1:n.*209+1_*209+2insCG
ENST00000695541.1:c.157+1_157+2insCG (IGF2)	ENSP00000511997.1:n.157+1_157+2insCG
ENST00000416167.7:c.157+1_157+2insCG (IGF2) MANE Select	ENSP00000414497.2:n.157+1_157+2insCG
ENST00000643349.1:c.*209+1_*209+2insCG	ENSP00000495715.1:n.*209+1_*209+2insCG
ENST00000356578.8:c.*209+1_*209+2insCG (INS-IGF2)	ENSP00000348986.4:n.*209+1_*209+2insCG
ENST00000381389.5:c.157+1_157+2insCG (IGF2)	ENSP00000370796.1:n.157+1_157+2insCG
ENST00000381392.5:c.157+1_157+2insCG (IGF2)	ENSP00000370799.1:n.157+1_157+2insCG
ENST00000381395.5:c.157+1_157+2insCG (IGF2)	ENSP00000370802.1:n.157+1_157+2insCG
ENST00000381406.8:c.157+1_157+2insCG (IGF2)	ENSP00000370813.4:n.157+1_157+2insCG
ENST00000416167.6:c.157+1_157+2insCG (IGF2)	ENSP00000414497.2:n.157+1_157+2insCG
ENST00000418738.2:c.157+1_157+2insCG (IGF2)	ENSP00000402047.2:n.157+1_157+2insCG
ENST00000434045.6:c.325+1_325+2insCG (IGF2)	ENSP00000391826.2:n.325+1_325+2insCG
NM_000612.5:c.157+1_157+2insCG (IGF2)	NP_000603.1:n.157+1_157+2insCG
NM_001007139.5:c.157+1_157+2insCG (IGF2)	NP_001007140.2:n.157+1_157+2insCG
NM_001127598.2:c.325+1_325+2insCG (IGF2)	NP_001121070.1:n.325+1_325+2insCG
NM_001291861.2:c.157+1_157+2insCG (IGF2)	NP_001278790.1:n.157+1_157+2insCG
NM_001291862.2:c.157+1_157+2insCG (IGF2)	NP_001278791.1:n.157+1_157+2insCG
NR_003512.3:n.871+1_871+2insCG (INS-IGF2)
NM_000612.6:c.157+1_157+2insCG (IGF2) MANE Select	NP_000603.1:n.157+1_157+2insCG
NM_001127598.3:c.325+1_325+2insCG (IGF2)	NP_001121070.1:n.325+1_325+2insCG
NM_001291861.3:c.157+1_157+2insCG (IGF2)	NP_001278790.1:n.157+1_157+2insCG
NM_001291862.3:c.157+1_157+2insCG (IGF2)	NP_001278791.1:n.157+1_157+2insCG
NR_003512.4:n.871+1_871+2insCG (INS-IGF2)
NM_001007139.6:c.157+1_157+2insCG (IGF2)	NP_001007140.2:n.157+1_157+2insCG