Canonical Allele Identifier: CA597088610
Gene: INS HGNC NCBI
INS-IGF2 HGNC NCBI

Linked Data

dbSNP Id: rs1369317193

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2159972_2159983del , CM000673.2:g.2159972_2159983del GRCh38
NC_000011.9:g.2181202_2181213del , CM000673.1:g.2181202_2181213del GRCh37
NC_000011.8:g.2137778_2137789del NCBI36
NG_007114.1:g.6213_6224del
NG_050578.1:g.6228_6239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381330.5:c.203_214del (INS) MANE Select ENSP00000370731.5:p.Leu68_Gly71del
ENST00000250971.7:c.203_214del (INS) ENSP00000250971.3:p.Leu68_Gly71del
ENST00000356578.8:c.187+803_187+814del (INS-IGF2) ENSP00000348986.4:n.187+803_187+814del
ENST00000381330.4:c.203_214del (INS) ENSP00000370731.4:p.Leu68_Gly71del
ENST00000397262.5:c.203_214del (INS) ENSP00000380432.1:p.Leu68_Gly71del
ENST00000397270.1:c.187+803_187+814del (INS-IGF2) ENSP00000380440.1:n.187+803_187+814del
ENST00000421783.1:c.188-110_188-99del (INS) ENSP00000408400.1:n.188-110_188-99del
ENST00000512523.1:c.188-21_188-10del (INS) ENSP00000424008.1:n.188-21_188-10del
NM_000207.2:c.203_214del (INS) NP_000198.1:p.Leu68_Gly71del
NM_001042376.2:c.187+803_187+814del (INS-IGF2) NP_001035835.1:n.187+803_187+814del
NM_001185097.1:c.203_214del (INS) NP_001172026.1:p.Leu68_Gly71del
NM_001185098.1:c.203_214del (INS) NP_001172027.1:p.Leu68_Gly71del
NM_001291897.1:c.203_214del (INS) NP_001278826.1:p.Leu68_Gly71del
NR_003512.3:n.246+803_246+814del (INS-IGF2)
NM_000207.3:c.203_214del (INS) MANE Select NP_000198.1:p.Leu68_Gly71del
NM_001042376.3:c.187+803_187+814del (INS-IGF2) NP_001035835.1:n.187+803_187+814del
NM_001185097.2:c.203_214del (INS) NP_001172026.1:p.Leu68_Gly71del
NM_001291897.2:c.203_214del (INS) NP_001278826.1:p.Leu68_Gly71del
NR_003512.4:n.246+803_246+814del (INS-IGF2)
NM_001185098.2:c.203_214del (INS) NP_001172027.1:p.Leu68_Gly71del