Canonical Allele Identifier: CA1226666397
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702629T= , CM000663.2:g.230702629T= GRCh38
NC_000001.10:g.230838375T= , CM000663.1:g.230838375T= GRCh37
NC_000001.9:g.228904998T= NCBI36
NG_008836.1:g.16962A=
NG_008836.2:g.16962A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.*512A= MANE Select ENSP00000355627.5:n.*512A=
ENST00000679738.1:c.*512A= ENSP00000505063.1:n.*512A=
ENST00000679802.1:c.*1402A= ENSP00000505184.1:n.*1402A=
ENST00000679854.1:n.6248A=
ENST00000680041.1:c.*512A= ENSP00000504866.1:n.*512A=
ENST00000680783.1:c.829+7366A= ENSP00000506329.1:n.829+7366A=
ENST00000681269.1:c.*512A= ENSP00000505985.1:n.*512A=
ENST00000681347.1:n.4049A=
ENST00000681514.1:c.*512A= ENSP00000505963.1:n.*512A=
ENST00000681772.1:c.*1437A= ENSP00000505829.1:n.*1437A=
ENST00000366667.4:c.*512A= ENSP00000355627.4:n.*512A=
NM_000029.3:c.*512A= NP_000020.1:n.*512A=
NM_000029.4:c.*512A= NP_000020.1:n.*512A=
NM_001382817.3:c.*512A= NP_001369746.2:n.*512A=
NM_001384479.1:c.*512A= MANE Select NP_001371408.1:n.*512A=