Canonical Allele Identifier: CA1226667775
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705945T= , CM000663.2:g.230705945T= GRCh38
NC_000001.10:g.230841691T= , CM000663.1:g.230841691T= GRCh37
NC_000001.9:g.228908314T= NCBI36
NG_008836.1:g.13646A=
NG_008836.2:g.13646A=

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1085A= MANE Select ENSP00000355627.5:p.Lys362=
ENST00000679684.1:c.1085A= ENSP00000505981.1:p.Lys362=
ENST00000679738.1:c.1085A= ENSP00000505063.1:p.Lys362=
ENST00000679802.1:c.*544A= ENSP00000505184.1:n.*544A=
ENST00000679854.1:n.5390A=
ENST00000679957.1:c.1085A= ENSP00000506646.1:p.Lys362=
ENST00000680041.1:c.1085A= ENSP00000504866.1:p.Lys362=
ENST00000680783.1:c.829+4050A= ENSP00000506329.1:n.829+4050A=
ENST00000681269.1:c.1085A= ENSP00000505985.1:p.Lys362=
ENST00000681347.1:n.1596A=
ENST00000681514.1:c.1085A= ENSP00000505963.1:p.Lys362=
ENST00000681772.1:c.1085A= ENSP00000505829.1:p.Lys362=
ENST00000366667.4:c.1112A= ENSP00000355627.4:p.Lys371=
NM_000029.3:c.1112A= NP_000020.1:p.Lys371=
NM_000029.4:c.1112A= NP_000020.1:p.Lys371=
NM_001382817.3:c.1085A= NP_001369746.2:p.Lys362=
NM_001384479.1:c.1085A= MANE Select NP_001371408.1:p.Lys362=