Canonical Allele Identifier: CA2611975021

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2149416-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2149416C>A , CM000673.2:g.2149416C>A	GRCh38
NC_000011.9:g.2170646C>A , CM000673.1:g.2170646C>A	GRCh37
NC_000011.8:g.2127222C>A	NCBI36
NG_008849.1:g.5188G>T
NG_050578.1:g.16794G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-468-71G>T (IGF2)	ENSP00000511998.1:n.-468-71G>T
ENST00000643349.2:c.-37G>T	ENSP00000495715.1:n.-37G>T
ENST00000695541.1:c.-469+56G>T (IGF2)	ENSP00000511997.1:n.-469+56G>T
ENST00000481781.2:n.126-71G>T
ENST00000643349.1:c.-37G>T	ENSP00000495715.1:n.-37G>T
ENST00000356578.8:c.188-71G>T (INS-IGF2)	ENSP00000348986.4:n.188-71G>T
ENST00000397270.1:c.188-71G>T (INS-IGF2)	ENSP00000380440.1:n.188-71G>T
ENST00000476874.1:n.71-71G>T (INS-IGF2)
ENST00000481781.1:n.393-71G>T (INS-IGF2)
NM_001007139.5:c.-539G>T (IGF2)	NP_001007140.2:n.-539G>T
NM_001042376.2:c.188-71G>T (INS-IGF2)	NP_001035835.1:n.188-71G>T
NR_003512.3:n.247-71G>T (INS-IGF2)
NM_001042376.3:c.188-71G>T (INS-IGF2)	NP_001035835.1:n.188-71G>T
NR_003512.4:n.247-71G>T (INS-IGF2)
NM_001007139.6:c.-539G>T (IGF2)	NP_001007140.2:n.-539G>T