Canonical Allele Identifier: CA216245449

Gene: IGF2 INS-IGF2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2132404T>G , CM000673.2:g.2132404T>G	GRCh38
NC_000011.9:g.2153634T>G , CM000673.1:g.2153634T>G	GRCh37
NC_000011.8:g.2110210T>G	NCBI36
NG_008849.1:g.22200A>C
NG_050578.1:g.33806A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643349.2:c.*1178A>C	ENSP00000495715.1:n.*1178A>C
ENST00000695541.1:c.*583A>C (IGF2)	ENSP00000511997.1:n.*583A>C
ENST00000416167.7:c.*583A>C (IGF2) MANE Select	ENSP00000414497.2:n.*583A>C
ENST00000643349.1:c.*1178A>C	ENSP00000495715.1:n.*1178A>C
ENST00000381395.5:c.*583A>C (IGF2)	ENSP00000370802.1:n.*583A>C
ENST00000381406.8:c.*583A>C (IGF2)	ENSP00000370813.4:n.*583A>C
ENST00000416167.6:c.*583A>C (IGF2)	ENSP00000414497.2:n.*583A>C
NM_000612.5:c.*583A>C (IGF2)	NP_000603.1:n.*583A>C
NM_001007139.5:c.*583A>C (IGF2)	NP_001007140.2:n.*583A>C
NM_001127598.2:c.*583A>C (IGF2)	NP_001121070.1:n.*583A>C
NM_001291861.2:c.*583A>C (IGF2)	NP_001278790.1:n.*583A>C
NM_001291862.2:c.*583A>C (IGF2)	NP_001278791.1:n.*583A>C
NR_003512.3:n.1840A>C (INS-IGF2)
NM_000612.6:c.*583A>C (IGF2) MANE Select	NP_000603.1:n.*583A>C
NM_001127598.3:c.*583A>C (IGF2)	NP_001121070.1:n.*583A>C
NM_001291861.3:c.*583A>C (IGF2)	NP_001278790.1:n.*583A>C
NM_001291862.3:c.*583A>C (IGF2)	NP_001278791.1:n.*583A>C
NR_003512.4:n.1840A>C (INS-IGF2)
NM_001007139.6:c.*583A>C (IGF2)	NP_001007140.2:n.*583A>C