Canonical Allele Identifier: CA379118531

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149271-C-T
• MyVariant Identifiers: chr11:g.2170501C>T (hg19) ; chr11:g.2149271C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-394G>A (IGF2)	ENSP00000511998.1:n.-394G>A
ENST00000643349.2:c.109G>A	ENSP00000495715.1:p.Ala37Thr
ENST00000695541.1:c.-394G>A (IGF2)	ENSP00000511997.1:n.-394G>A
ENST00000481781.2:n.200G>A
ENST00000643349.1:c.109G>A	ENSP00000495715.1:p.Ala37Thr
ENST00000356578.8:c.262G>A (INS-IGF2)	ENSP00000348986.4:p.Ala88Thr
ENST00000397270.1:c.262G>A (INS-IGF2)	ENSP00000380440.1:p.Ala88Thr
ENST00000476874.1:n.145G>A (INS-IGF2)
ENST00000481781.1:n.467G>A (INS-IGF2)
NM_001007139.5:c.-394G>A (IGF2)	NP_001007140.2:n.-394G>A
NM_001042376.2:c.262G>A (INS-IGF2)	NP_001035835.1:p.Ala88Thr
NR_003512.3:n.321G>A (INS-IGF2)
NM_001042376.3:c.262G>A (INS-IGF2)	NP_001035835.1:p.Ala88Thr
NR_003512.4:n.321G>A (INS-IGF2)
NM_001007139.6:c.-394G>A (IGF2)	NP_001007140.2:n.-394G>A