Canonical Allele Identifier: CA379118533

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170501C>A (hg19) ; chr11:g.2149271C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149271C>A , CM000673.2:g.2149271C>A	GRCh38
NC_000011.9:g.2170501C>A , CM000673.1:g.2170501C>A	GRCh37
NC_000011.8:g.2127077C>A	NCBI36
NG_008849.1:g.5333G>T
NG_050578.1:g.16939G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-394G>T (IGF2)	ENSP00000511998.1:n.-394G>T
ENST00000643349.2:c.109G>T	ENSP00000495715.1:p.Ala37Ser
ENST00000695541.1:c.-394G>T (IGF2)	ENSP00000511997.1:n.-394G>T
ENST00000481781.2:n.200G>T
ENST00000643349.1:c.109G>T	ENSP00000495715.1:p.Ala37Ser
ENST00000356578.8:c.262G>T (INS-IGF2)	ENSP00000348986.4:p.Ala88Ser
ENST00000397270.1:c.262G>T (INS-IGF2)	ENSP00000380440.1:p.Ala88Ser
ENST00000476874.1:n.145G>T (INS-IGF2)
ENST00000481781.1:n.467G>T (INS-IGF2)
NM_001007139.5:c.-394G>T (IGF2)	NP_001007140.2:n.-394G>T
NM_001042376.2:c.262G>T (INS-IGF2)	NP_001035835.1:p.Ala88Ser
NR_003512.3:n.321G>T (INS-IGF2)
NM_001042376.3:c.262G>T (INS-IGF2)	NP_001035835.1:p.Ala88Ser
NR_003512.4:n.321G>T (INS-IGF2)
NM_001007139.6:c.-394G>T (IGF2)	NP_001007140.2:n.-394G>T