Canonical Allele Identifier: CA10638760

Gene: INS INS-IGF2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2161163_2161164insGCAA , CM000673.2:g.2161163_2161164insGCAA	GRCh38
NC_000011.9:g.2182393_2182394insGCAA , CM000673.1:g.2182393_2182394insGCAA	GRCh37
NC_000011.8:g.2138969_2138970insGCAA	NCBI36
NG_007114.1:g.5031_5032insTTGC
NG_050578.1:g.5046_5047insTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381330.5:c.-18+4_-18+5insTTGC (INS) MANE Select	ENSP00000370731.5:n.-18+4_-18+5insTTGC
ENST00000250971.7:c.-40_-39insTTGC (INS)	ENSP00000250971.3:n.-40_-39insTTGC
ENST00000356578.8:c.-18+4_-18+5insTTGC (INS-IGF2)	ENSP00000348986.4:n.-18+4_-18+5insTTGC
ENST00000381330.4:c.-18+4_-18+5insTTGC (INS)	ENSP00000370731.4:n.-18+4_-18+5insTTGC
ENST00000397262.5:c.-193_-192insTTGC (INS)	ENSP00000380432.1:n.-193_-192insTTGC
ENST00000397270.1:c.-18+4_-18+5insTTGC (INS-IGF2)	ENSP00000380440.1:n.-18+4_-18+5insTTGC
NM_000207.2:c.-18+4_-18+5insTTGC (INS)	NP_000198.1:n.-18+4_-18+5insTTGC
NM_001042376.2:c.-18+4_-18+5insTTGC (INS-IGF2)	NP_001035835.1:n.-18+4_-18+5insTTGC
NM_001185097.1:c.-40_-39insTTGC (INS)	NP_001172026.1:n.-40_-39insTTGC
NM_001185098.1:c.-193_-192insTTGC (INS)	NP_001172027.1:n.-193_-192insTTGC
NM_001291897.1:c.-74_-73insTTGC (INS)	NP_001278826.1:n.-74_-73insTTGC
NR_003512.3:n.42+4_42+5insTTGC (INS-IGF2)
NM_000207.3:c.-18+4_-18+5insTTGC (INS) MANE Select	NP_000198.1:n.-18+4_-18+5insTTGC
NM_001042376.3:c.-18+4_-18+5insTTGC (INS-IGF2)	NP_001035835.1:n.-18+4_-18+5insTTGC
NM_001185097.2:c.-40_-39insTTGC (INS)	NP_001172026.1:n.-40_-39insTTGC
NM_001291897.2:c.-74_-73insTTGC (INS)	NP_001278826.1:n.-74_-73insTTGC
NR_003512.4:n.42+4_42+5insTTGC (INS-IGF2)
NM_001185098.2:c.-193_-192insTTGC (INS)	NP_001172027.1:n.-193_-192insTTGC