Canonical Allele Identifier: CA1226661615
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230713515_230713519delinsATTAG , CM000663.2:g.230713515_230713519delinsATTAG GRCh38
NC_000001.10:g.230849261_230849265delinsATTAG , CM000663.1:g.230849261_230849265delinsATTAG GRCh37
NC_000001.9:g.228915884_228915888delinsATTAG NCBI36
NG_008836.1:g.6072_6076delinsCTAAT
NG_008836.2:g.6072_6076delinsCTAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.-31+567_-31+571delinsCTAAT MANE Select ENSP00000355627.5:n.-31+567_-31+571delins...
ENST00000679684.1:c.-31+567_-31+571delinsCTAAT ENSP00000505981.1:n.-31+567_-31+571delins...
ENST00000679738.1:c.-31+567_-31+571delinsCTAAT ENSP00000505063.1:n.-31+567_-31+571delins...
ENST00000679802.1:c.-31+567_-31+571delinsCTAAT ENSP00000505184.1:n.-31+567_-31+571delins...
ENST00000679854.1:n.481+567_481+571delinsCTAAT
ENST00000679957.1:c.-31+567_-31+571delinsCTAAT ENSP00000506646.1:n.-31+567_-31+571delins...
ENST00000680041.1:c.-156+567_-156+571delinsCTAAT ENSP00000504866.1:n.-156+567_-156+571deli...
ENST00000680783.1:c.-31+567_-31+571delinsCTAAT ENSP00000506329.1:n.-31+567_-31+571delins...
ENST00000681269.1:c.-30-2666_-30-2662delinsCTAAT ENSP00000505985.1:n.-30-2666_-30-2662deli...
ENST00000681347.1:n.481+567_481+571delinsCTAAT
ENST00000681514.1:c.-117-150_-117-146delinsCTAAT ENSP00000505963.1:n.-117-150_-117-146deli...
ENST00000681772.1:c.-31+567_-31+571delinsCTAAT ENSP00000505829.1:n.-31+567_-31+571delins...
ENST00000366667.4:c.-4+567_-4+571delinsCTAAT ENSP00000355627.4:n.-4+567_-4+571delinsCT...
NM_000029.3:c.-4+567_-4+571delinsCTAAT NP_000020.1:n.-4+567_-4+571delinsCTAAT
NM_000029.4:c.-4+567_-4+571delinsCTAAT NP_000020.1:n.-4+567_-4+571delinsCTAAT
NM_001382817.3:c.-30-2666_-30-2662delinsCTAAT NP_001369746.2:n.-30-2666_-30-2662delinsC...
NM_001384479.1:c.-31+567_-31+571delinsCTAAT MANE Select NP_001371408.1:n.-31+567_-31+571delinsCTA...