Canonical Allele Identifier: CA2611973434

Gene: IGF2 INS-IGF2

Linked Data

• gnomAD v4: 11-2148941-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2148941G>T , CM000673.2:g.2148941G>T	GRCh38
NC_000011.9:g.2170171G>T , CM000673.1:g.2170171G>T	GRCh37
NC_000011.8:g.2126747G>T	NCBI36
NG_008849.1:g.5663C>A
NG_050578.1:g.17269C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000481781.3:c.-249+185C>A (IGF2)	ENSP00000511998.1:n.-249+185C>A
ENST00000643349.2:c.254+185C>A	ENSP00000495715.1:n.254+185C>A
ENST00000695541.1:c.-249+185C>A (IGF2)	ENSP00000511997.1:n.-249+185C>A
ENST00000481781.2:n.345+185C>A
ENST00000643349.1:c.254+185C>A	ENSP00000495715.1:n.254+185C>A
ENST00000356578.8:c.407+185C>A (INS-IGF2)	ENSP00000348986.4:n.407+185C>A
ENST00000397270.1:c.407+185C>A (INS-IGF2)	ENSP00000380440.1:n.407+185C>A
ENST00000476874.1:n.475C>A (INS-IGF2)
ENST00000481781.1:n.612+185C>A (INS-IGF2)
NM_001007139.5:c.-249+185C>A (IGF2)	NP_001007140.2:n.-249+185C>A
NM_001042376.2:c.407+185C>A (INS-IGF2)	NP_001035835.1:n.407+185C>A
NR_003512.3:n.466+185C>A (INS-IGF2)
NM_001042376.3:c.407+185C>A (INS-IGF2)	NP_001035835.1:n.407+185C>A
NR_003512.4:n.466+185C>A (INS-IGF2)
NM_001007139.6:c.-249+185C>A (IGF2)	NP_001007140.2:n.-249+185C>A