Canonical Allele Identifier: CA1226667771
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705940A= , CM000663.2:g.230705940A= GRCh38
NC_000001.10:g.230841686A= , CM000663.1:g.230841686A= GRCh37
NC_000001.9:g.228908309A= NCBI36
NG_008836.1:g.13651T=
NG_008836.2:g.13651T=

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1090T= MANE Select ENSP00000355627.5:p.Ser364=
ENST00000679684.1:c.1090T= ENSP00000505981.1:p.Ser364=
ENST00000679738.1:c.1090T= ENSP00000505063.1:p.Ser364=
ENST00000679802.1:c.*549T= ENSP00000505184.1:p.=
ENST00000679854.1:n.5395T=
ENST00000679957.1:c.1090T= ENSP00000506646.1:p.Ser364=
ENST00000680041.1:c.1090T= ENSP00000504866.1:p.Ser364=
ENST00000680783.1:c.829+4055T= ENSP00000506329.1:p.=
ENST00000681269.1:c.1090T= ENSP00000505985.1:p.Ser364=
ENST00000681347.1:n.1601T=
ENST00000681514.1:c.1090T= ENSP00000505963.1:p.Ser364=
ENST00000681772.1:c.1090T= ENSP00000505829.1:p.Ser364=
ENST00000366667.4:c.1117T= ENSP00000355627.4:p.Ser373=
NM_000029.3:c.1117T= NP_000020.1:p.Ser373=
NM_000029.4:c.1117T= NP_000020.1:p.Ser373=
NM_001382817.3:c.1090T= NP_001369746.2:p.Ser364=
NM_001384479.1:c.1090T= MANE Select NP_001371408.1:p.Ser364=