Canonical Allele Identifier: CA2611971837
Gene: IGF2 HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

gnomAD v4: 11-2148685-T-TGACG
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2148685_2148686insGACG , CM000673.2:g.2148685_2148686insGACG GRCh38
NC_000011.9:g.2169915_2169916insGACG , CM000673.1:g.2169915_2169916insGACG GRCh37
NC_000011.8:g.2126491_2126492insGACG NCBI36
NG_008849.1:g.5918_5919insCGTC
NG_050578.1:g.17524_17525insCGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000481781.3:c.-249+440_-249+441insCGTC (IGF2) ENSP00000511998.1:n.-249+440_-249+441insCGTC
ENST00000643349.2:c.254+440_254+441insCGTC ENSP00000495715.1:n.254+440_254+441insCGTC
ENST00000695541.1:c.-249+440_-249+441insCGTC (IGF2) ENSP00000511997.1:n.-249+440_-249+441insCGTC
ENST00000481781.2:n.345+440_345+441insCGTC
ENST00000643349.1:c.254+440_254+441insCGTC ENSP00000495715.1:n.254+440_254+441insCGTC
ENST00000356578.8:c.407+440_407+441insCGTC (INS-IGF2) ENSP00000348986.4:n.407+440_407+441insCGTC
ENST00000397270.1:c.407+440_407+441insCGTC (INS-IGF2) ENSP00000380440.1:n.407+440_407+441insCGTC
ENST00000481781.1:n.612+440_612+441insCGTC (INS-IGF2)
NM_001007139.5:c.-249+440_-249+441insCGTC (IGF2) NP_001007140.2:n.-249+440_-249+441insCGTC
NM_001042376.2:c.407+440_407+441insCGTC (INS-IGF2) NP_001035835.1:n.407+440_407+441insCGTC
NR_003512.3:n.466+440_466+441insCGTC (INS-IGF2)
NM_001042376.3:c.407+440_407+441insCGTC (INS-IGF2) NP_001035835.1:n.407+440_407+441insCGTC
NR_003512.4:n.466+440_466+441insCGTC (INS-IGF2)
NM_001007139.6:c.-249+440_-249+441insCGTC (IGF2) NP_001007140.2:n.-249+440_-249+441insCGTC
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