Canonical Allele Identifier: CA2650971414
Gene: AGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710369_230710370del , CM000663.2:g.230710369_230710370del GRCh38
NC_000001.10:g.230846115_230846116del , CM000663.1:g.230846115_230846116del GRCh37
NC_000001.9:g.228912738_228912739del NCBI36
NG_008836.1:g.9221_9222del
NG_008836.2:g.9221_9222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.454_455del MANE Select ENSP00000355627.5:p.Ile152ProfsTer?
ENST00000679684.1:c.454_455del ENSP00000505981.1:p.Ile152ProfsTer?
ENST00000679738.1:c.454_455del ENSP00000505063.1:p.Ile152ProfsTer?
ENST00000679802.1:c.454_455del ENSP00000505184.1:p.Ile152ProfsTer?
ENST00000679854.1:n.965_966del
ENST00000679957.1:c.454_455del ENSP00000506646.1:p.Ile152ProfsTer?
ENST00000680041.1:c.454_455del ENSP00000504866.1:p.Ile152ProfsTer?
ENST00000680783.1:c.454_455del ENSP00000506329.1:p.Ile152ProfsTer?
ENST00000681269.1:c.454_455del ENSP00000505985.1:p.Ile152ProfsTer?
ENST00000681347.1:n.965_966del
ENST00000681514.1:c.454_455del ENSP00000505963.1:p.Ile152ProfsTer?
ENST00000681772.1:c.454_455del ENSP00000505829.1:p.Ile152ProfsTer?
ENST00000366667.4:c.481_482del ENSP00000355627.4:p.Ile161ProfsTer?
NM_000029.3:c.481_482del NP_000020.1:p.Ile161ProfsTer?
NM_000029.4:c.481_482del NP_000020.1:p.Ile161ProfsTer?
NM_001382817.3:c.454_455del NP_001369746.2:p.Ile152ProfsTer?
NM_001384479.1:c.454_455del MANE Select NP_001371408.1:p.Ile152ProfsTer?