Canonical Allele Identifier: CA597431415

Gene: IGF2 INS-IGF2

Linked Data

• dbSNP Id: rs2230949
• gnomAD v2: 11-2154188-G-C
• gnomAD v4: 11-2132958-G-C
• MyVariant Identifiers: chr11:g.2154188G>C (hg19) ; chr11:g.2132958G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2132958G>C , CM000673.2:g.2132958G>C	GRCh38
NC_000011.9:g.2154188G>C , CM000673.1:g.2154188G>C	GRCh37
NC_000011.8:g.2110764G>C	NCBI36
NG_008849.1:g.21646C>G
NG_050578.1:g.33252C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.*29C>G (IGF2)	ENSP00000511998.1:n.*29C>G
ENST00000643349.2:c.*624C>G	ENSP00000495715.1:n.*624C>G
ENST00000695541.1:c.*29C>G (IGF2)	ENSP00000511997.1:n.*29C>G
ENST00000416167.7:c.*29C>G (IGF2) MANE Select	ENSP00000414497.2:n.*29C>G
ENST00000643349.1:c.*624C>G	ENSP00000495715.1:n.*624C>G
ENST00000356578.8:c.*624C>G (INS-IGF2)	ENSP00000348986.4:n.*624C>G
ENST00000381389.5:c.*29C>G (IGF2)	ENSP00000370796.1:n.*29C>G
ENST00000381392.5:c.*29C>G (IGF2)	ENSP00000370799.1:n.*29C>G
ENST00000381395.5:c.*29C>G (IGF2)	ENSP00000370802.1:n.*29C>G
ENST00000381406.8:c.*29C>G (IGF2)	ENSP00000370813.4:n.*29C>G
ENST00000416167.6:c.*29C>G (IGF2)	ENSP00000414497.2:n.*29C>G
ENST00000418738.2:c.*29C>G (IGF2)	ENSP00000402047.2:n.*29C>G
ENST00000434045.6:c.*29C>G (IGF2)	ENSP00000391826.2:n.*29C>G
NM_000612.5:c.*29C>G (IGF2)	NP_000603.1:n.*29C>G
NM_001007139.5:c.*29C>G (IGF2)	NP_001007140.2:n.*29C>G
NM_001127598.2:c.*29C>G (IGF2)	NP_001121070.1:n.*29C>G
NM_001291861.2:c.*29C>G (IGF2)	NP_001278790.1:n.*29C>G
NM_001291862.2:c.*29C>G (IGF2)	NP_001278791.1:n.*29C>G
NR_003512.3:n.1286C>G (INS-IGF2)
NM_000612.6:c.*29C>G (IGF2) MANE Select	NP_000603.1:n.*29C>G
NM_001127598.3:c.*29C>G (IGF2)	NP_001121070.1:n.*29C>G
NM_001291861.3:c.*29C>G (IGF2)	NP_001278790.1:n.*29C>G
NM_001291862.3:c.*29C>G (IGF2)	NP_001278791.1:n.*29C>G
NR_003512.4:n.1286C>G (INS-IGF2)
NM_001007139.6:c.*29C>G (IGF2)	NP_001007140.2:n.*29C>G