Canonical Allele Identifier: CA5817794

Gene: IGF2 INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2140200G>A , CM000673.2:g.2140200G>A	GRCh38
NC_000011.9:g.2161430G>A , CM000673.1:g.2161430G>A	GRCh37
NC_000011.8:g.2118006G>A	NCBI36
NG_008849.1:g.14404C>T
NG_050578.1:g.26010C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001007139.5:c.-6-4671C>T (IGF2)	NP_001007140.2:n.-6-4671C>T
NM_001007139.6:c.-6-4671C>T (IGF2)	NP_001007140.2:n.-6-4671C>T
NM_001127598.2:c.97C>T (IGF2)	NP_001121070.1:p.Gln33Ter
NM_001127598.3:c.97C>T (IGF2)	NP_001121070.1:p.Gln33Ter
NM_001291862.2:c.-7+657C>T (IGF2)	NP_001278791.1:n.-7+657C>T
NM_001291862.3:c.-7+657C>T (IGF2)	NP_001278791.1:n.-7+657C>T
NR_003512.3:n.709-4671C>T (INS-IGF2)
NR_003512.4:n.709-4671C>T (INS-IGF2)
ENST00000356578.8:c.*47-4671C>T (INS-IGF2)	ENSP00000348986.4:n.*47-4671C>T
ENST00000381389.5:c.-7+657C>T (IGF2)	ENSP00000370796.1:n.-7+657C>T
ENST00000434045.6:c.97C>T (IGF2)	ENSP00000391826.2:p.Gln33Ter
ENST00000481781.3:c.-6-4671C>T (IGF2)	ENSP00000511998.1:n.-6-4671C>T
ENST00000643349.1:c.*47-4671C>T	ENSP00000495715.1:n.*47-4671C>T
ENST00000643349.2:c.*47-4671C>T	ENSP00000495715.1:n.*47-4671C>T
ENST00000695541.1:c.-6-4671C>T (IGF2)	ENSP00000511997.1:n.-6-4671C>T