Canonical Allele Identifier: CA1948025838
Gene: INS HGNC NCBI
INS-IGF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2159823G= , CM000673.2:g.2159823G= GRCh38
NC_000011.9:g.2181053G= , CM000673.1:g.2181053G= GRCh37
NC_000011.8:g.2137629G= NCBI36
NG_007114.1:g.6372C=
NG_050578.1:g.6387C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381330.5:c.*29C= (INS) MANE Select ENSP00000370731.5:n.*29C=
ENST00000250971.7:c.*29C= (INS) ENSP00000250971.3:n.*29C=
ENST00000356578.8:c.187+962C= (INS-IGF2) ENSP00000348986.4:n.187+962C=
ENST00000381330.4:c.*29C= (INS) ENSP00000370731.4:n.*29C=
ENST00000397262.5:c.*29C= (INS) ENSP00000380432.1:n.*29C=
ENST00000397270.1:c.187+962C= (INS-IGF2) ENSP00000380440.1:n.187+962C=
ENST00000421783.1:c.237C= (INS) ENSP00000408400.1:p.Arg79=
NM_000207.2:c.*29C= (INS) NP_000198.1:n.*29C=
NM_001042376.2:c.187+962C= (INS-IGF2) NP_001035835.1:n.187+962C=
NM_001185097.1:c.*29C= (INS) NP_001172026.1:n.*29C=
NM_001185098.1:c.*29C= (INS) NP_001172027.1:n.*29C=
NM_001291897.1:c.*29C= (INS) NP_001278826.1:n.*29C=
NR_003512.3:n.246+962C= (INS-IGF2)
NM_000207.3:c.*29C= (INS) MANE Select NP_000198.1:n.*29C=
NM_001042376.3:c.187+962C= (INS-IGF2) NP_001035835.1:n.187+962C=
NM_001185097.2:c.*29C= (INS) NP_001172026.1:n.*29C=
NM_001291897.2:c.*29C= (INS) NP_001278826.1:n.*29C=
NR_003512.4:n.246+962C= (INS-IGF2)
NM_001185098.2:c.*29C= (INS) NP_001172027.1:n.*29C=