Canonical Allele Identifier: CA2841911313

Gene: INS INS-IGF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2159826G>A , CM000673.2:g.2159826G>A	GRCh38
NC_000011.9:g.2181056G>A , CM000673.1:g.2181056G>A	GRCh37
NC_000011.8:g.2137632G>A	NCBI36
NG_007114.1:g.6369C>T
NG_050578.1:g.6384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381330.5:c.*26C>T (INS) MANE Select	ENSP00000370731.5:n.*26C>T
ENST00000250971.7:c.*26C>T (INS)	ENSP00000250971.3:n.*26C>T
ENST00000356578.8:c.187+959C>T (INS-IGF2)	ENSP00000348986.4:n.187+959C>T
ENST00000381330.4:c.*26C>T (INS)	ENSP00000370731.4:n.*26C>T
ENST00000397262.5:c.*26C>T (INS)	ENSP00000380432.1:n.*26C>T
ENST00000397270.1:c.187+959C>T (INS-IGF2)	ENSP00000380440.1:n.187+959C>T
ENST00000421783.1:c.234C>T (INS)	ENSP00000408400.1:p.Thr78=
NM_000207.2:c.*26C>T (INS)	NP_000198.1:n.*26C>T
NM_001042376.2:c.187+959C>T (INS-IGF2)	NP_001035835.1:n.187+959C>T
NM_001185097.1:c.*26C>T (INS)	NP_001172026.1:n.*26C>T
NM_001185098.1:c.*26C>T (INS)	NP_001172027.1:n.*26C>T
NM_001291897.1:c.*26C>T (INS)	NP_001278826.1:n.*26C>T
NR_003512.3:n.246+959C>T (INS-IGF2)
NM_000207.3:c.*26C>T (INS) MANE Select	NP_000198.1:n.*26C>T
NM_001042376.3:c.187+959C>T (INS-IGF2)	NP_001035835.1:n.187+959C>T
NM_001185097.2:c.*26C>T (INS)	NP_001172026.1:n.*26C>T
NM_001291897.2:c.*26C>T (INS)	NP_001278826.1:n.*26C>T
NR_003512.4:n.246+959C>T (INS-IGF2)
NM_001185098.2:c.*26C>T (INS)	NP_001172027.1:n.*26C>T