Canonical Allele Identifier: CA379118320

Gene: IGF2 INS-IGF2

Linked Data

• MyVariant Identifiers: chr11:g.2170435C>A (hg19) ; chr11:g.2149205C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149205C>A , CM000673.2:g.2149205C>A	GRCh38
NC_000011.9:g.2170435C>A , CM000673.1:g.2170435C>A	GRCh37
NC_000011.8:g.2127011C>A	NCBI36
NG_008849.1:g.5399G>T
NG_050578.1:g.17005G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-328G>T (IGF2)	ENSP00000511998.1:n.-328G>T
ENST00000643349.2:c.175G>T	ENSP00000495715.1:p.Ala59Ser
ENST00000695541.1:c.-328G>T (IGF2)	ENSP00000511997.1:n.-328G>T
ENST00000481781.2:n.266G>T
ENST00000643349.1:c.175G>T	ENSP00000495715.1:p.Ala59Ser
ENST00000356578.8:c.328G>T (INS-IGF2)	ENSP00000348986.4:p.Ala110Ser
ENST00000397270.1:c.328G>T (INS-IGF2)	ENSP00000380440.1:p.Ala110Ser
ENST00000476874.1:n.211G>T (INS-IGF2)
ENST00000481781.1:n.533G>T (INS-IGF2)
NM_001007139.5:c.-328G>T (IGF2)	NP_001007140.2:n.-328G>T
NM_001042376.2:c.328G>T (INS-IGF2)	NP_001035835.1:p.Ala110Ser
NR_003512.3:n.387G>T (INS-IGF2)
NM_001042376.3:c.328G>T (INS-IGF2)	NP_001035835.1:p.Ala110Ser
NR_003512.4:n.387G>T (INS-IGF2)
NM_001007139.6:c.-328G>T (IGF2)	NP_001007140.2:n.-328G>T