Canonical Allele Identifier: CA2611972009

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2148712-G-GTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148712_2148713insTTT , CM000673.2:g.2148712_2148713insTTT	GRCh38
NC_000011.9:g.2169942_2169943insTTT , CM000673.1:g.2169942_2169943insTTT	GRCh37
NC_000011.8:g.2126518_2126519insTTT	NCBI36
NG_008849.1:g.5891_5892insAAA
NG_050578.1:g.17497_17498insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481781.3:c.-249+413_-249+414insAAA (IGF2)	ENSP00000511998.1:n.-249+413_-249+414insAAA
ENST00000643349.2:c.254+413_254+414insAAA	ENSP00000495715.1:n.254+413_254+414insAAA
ENST00000695541.1:c.-249+413_-249+414insAAA (IGF2)	ENSP00000511997.1:n.-249+413_-249+414insAAA
ENST00000481781.2:n.345+413_345+414insAAA
ENST00000643349.1:c.254+413_254+414insAAA	ENSP00000495715.1:n.254+413_254+414insAAA
ENST00000356578.8:c.407+413_407+414insAAA (INS-IGF2)	ENSP00000348986.4:n.407+413_407+414insAAA
ENST00000397270.1:c.407+413_407+414insAAA (INS-IGF2)	ENSP00000380440.1:n.407+413_407+414insAAA
ENST00000481781.1:n.612+413_612+414insAAA (INS-IGF2)
NM_001007139.5:c.-249+413_-249+414insAAA (IGF2)	NP_001007140.2:n.-249+413_-249+414insAAA
NM_001042376.2:c.407+413_407+414insAAA (INS-IGF2)	NP_001035835.1:n.407+413_407+414insAAA
NR_003512.3:n.466+413_466+414insAAA (INS-IGF2)
NM_001042376.3:c.407+413_407+414insAAA (INS-IGF2)	NP_001035835.1:n.407+413_407+414insAAA
NR_003512.4:n.466+413_466+414insAAA (INS-IGF2)
NM_001007139.6:c.-249+413_-249+414insAAA (IGF2)	NP_001007140.2:n.-249+413_-249+414insAAA