Canonical Allele Identifier: CA472029020

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170382C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149152C>G , CM000673.2:g.2149152C>G	GRCh38
NC_000011.9:g.2170382C>G , CM000673.1:g.2170382C>G	GRCh37
NC_000011.8:g.2126958C>G	NCBI36
NG_008849.1:g.5452G>C
NG_050578.1:g.17058G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-275G>C (IGF2)	ENSP00000511998.1:n.-275G>C
ENST00000643349.2:c.228G>C	ENSP00000495715.1:p.Ala76=
ENST00000695541.1:c.-275G>C (IGF2)	ENSP00000511997.1:n.-275G>C
ENST00000481781.2:n.319G>C
ENST00000643349.1:c.228G>C	ENSP00000495715.1:p.Ala76=
ENST00000356578.8:c.381G>C (INS-IGF2)	ENSP00000348986.4:p.Ala127=
ENST00000397270.1:c.381G>C (INS-IGF2)	ENSP00000380440.1:p.Ala127=
ENST00000476874.1:n.264G>C (INS-IGF2)
ENST00000481781.1:n.586G>C (INS-IGF2)
NM_001007139.5:c.-275G>C (IGF2)	NP_001007140.2:n.-275G>C
NM_001042376.2:c.381G>C (INS-IGF2)	NP_001035835.1:p.Ala127=
NR_003512.3:n.440G>C (INS-IGF2)
NM_001042376.3:c.381G>C (INS-IGF2)	NP_001035835.1:p.Ala127=
NR_003512.4:n.440G>C (INS-IGF2)
NM_001007139.6:c.-275G>C (IGF2)	NP_001007140.2:n.-275G>C