Canonical Allele Identifier: CA379118416

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149240-G-A
• MyVariant Identifiers: chr11:g.2170470G>A (hg19) ; chr11:g.2149240G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149240G>A , CM000673.2:g.2149240G>A	GRCh38
NC_000011.9:g.2170470G>A , CM000673.1:g.2170470G>A	GRCh37
NC_000011.8:g.2127046G>A	NCBI36
NG_008849.1:g.5364C>T
NG_050578.1:g.16970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-363C>T (IGF2)	ENSP00000511998.1:n.-363C>T
ENST00000643349.2:c.140C>T	ENSP00000495715.1:p.Ala47Val
ENST00000695541.1:c.-363C>T (IGF2)	ENSP00000511997.1:n.-363C>T
ENST00000481781.2:n.231C>T
ENST00000643349.1:c.140C>T	ENSP00000495715.1:p.Ala47Val
ENST00000356578.8:c.293C>T (INS-IGF2)	ENSP00000348986.4:p.Ala98Val
ENST00000397270.1:c.293C>T (INS-IGF2)	ENSP00000380440.1:p.Ala98Val
ENST00000476874.1:n.176C>T (INS-IGF2)
ENST00000481781.1:n.498C>T (INS-IGF2)
NM_001007139.5:c.-363C>T (IGF2)	NP_001007140.2:n.-363C>T
NM_001042376.2:c.293C>T (INS-IGF2)	NP_001035835.1:p.Ala98Val
NR_003512.3:n.352C>T (INS-IGF2)
NM_001042376.3:c.293C>T (INS-IGF2)	NP_001035835.1:p.Ala98Val
NR_003512.4:n.352C>T (INS-IGF2)
NM_001007139.6:c.-363C>T (IGF2)	NP_001007140.2:n.-363C>T