Canonical Allele Identifier: CA2611963353

Gene: INS INS-IGF2

Linked Data

• gnomAD v4: 11-2160734-AGCAGGGGGTGGCTGGGGGCGGCCAGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2160739_2160765del , CM000673.2:g.2160739_2160765del	GRCh38
NC_000011.9:g.2181969_2181995del , CM000673.1:g.2181969_2181995del	GRCh37
NC_000011.8:g.2138545_2138571del	NCBI36
NG_007114.1:g.5434_5460del
NG_050578.1:g.5449_5475del

Transcript Alleles

HGVS	Amino-acid change
ENST00000381330.5:c.187+24_187+50del (INS) MANE Select	ENSP00000370731.5:n.187+24_187+50del
ENST00000250971.7:c.187+24_187+50del (INS)	ENSP00000250971.3:n.187+24_187+50del
ENST00000356578.8:c.187+24_187+50del (INS-IGF2)	ENSP00000348986.4:n.187+24_187+50del
ENST00000381330.4:c.187+24_187+50del (INS)	ENSP00000370731.4:n.187+24_187+50del
ENST00000397262.5:c.187+24_187+50del (INS)	ENSP00000380432.1:n.187+24_187+50del
ENST00000397270.1:c.187+24_187+50del (INS-IGF2)	ENSP00000380440.1:n.187+24_187+50del
ENST00000421783.1:c.187+24_187+50del (INS)	ENSP00000408400.1:n.187+24_187+50del
ENST00000512523.1:c.187+24_187+50del (INS)	ENSP00000424008.1:n.187+24_187+50del
NM_000207.2:c.187+24_187+50del (INS)	NP_000198.1:n.187+24_187+50del
NM_001042376.2:c.187+24_187+50del (INS-IGF2)	NP_001035835.1:n.187+24_187+50del
NM_001185097.1:c.187+24_187+50del (INS)	NP_001172026.1:n.187+24_187+50del
NM_001185098.1:c.187+24_187+50del (INS)	NP_001172027.1:n.187+24_187+50del
NM_001291897.1:c.187+24_187+50del (INS)	NP_001278826.1:n.187+24_187+50del
NR_003512.3:n.246+24_246+50del (INS-IGF2)
NM_000207.3:c.187+24_187+50del (INS) MANE Select	NP_000198.1:n.187+24_187+50del
NM_001042376.3:c.187+24_187+50del (INS-IGF2)	NP_001035835.1:n.187+24_187+50del
NM_001185097.2:c.187+24_187+50del (INS)	NP_001172026.1:n.187+24_187+50del
NM_001291897.2:c.187+24_187+50del (INS)	NP_001278826.1:n.187+24_187+50del
NR_003512.4:n.246+24_246+50del (INS-IGF2)
NM_001185098.2:c.187+24_187+50del (INS)	NP_001172027.1:n.187+24_187+50del