Canonical Allele Identifier: CA472029002

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170376A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149146A>T , CM000673.2:g.2149146A>T	GRCh38
NC_000011.9:g.2170376A>T , CM000673.1:g.2170376A>T	GRCh37
NC_000011.8:g.2126952A>T	NCBI36
NG_008849.1:g.5458T>A
NG_050578.1:g.17064T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-269T>A (IGF2)	ENSP00000511998.1:n.-269T>A
ENST00000643349.2:c.234T>A	ENSP00000495715.1:p.Thr78=
ENST00000695541.1:c.-269T>A (IGF2)	ENSP00000511997.1:n.-269T>A
ENST00000481781.2:n.325T>A
ENST00000643349.1:c.234T>A	ENSP00000495715.1:p.Thr78=
ENST00000356578.8:c.387T>A (INS-IGF2)	ENSP00000348986.4:p.Thr129=
ENST00000397270.1:c.387T>A (INS-IGF2)	ENSP00000380440.1:p.Thr129=
ENST00000476874.1:n.270T>A (INS-IGF2)
ENST00000481781.1:n.592T>A (INS-IGF2)
NM_001007139.5:c.-269T>A (IGF2)	NP_001007140.2:n.-269T>A
NM_001042376.2:c.387T>A (INS-IGF2)	NP_001035835.1:p.Thr129=
NR_003512.3:n.446T>A (INS-IGF2)
NM_001042376.3:c.387T>A (INS-IGF2)	NP_001035835.1:p.Thr129=
NR_003512.4:n.446T>A (INS-IGF2)
NM_001007139.6:c.-269T>A (IGF2)	NP_001007140.2:n.-269T>A