Canonical Allele Identifier: CA1149053984

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703225G= , CM000663.2:g.230703225G=	GRCh38
NC_000001.10:g.230838971G= , CM000663.1:g.230838971G=	GRCh37
NC_000001.9:g.228905594G=	NCBI36
NG_008836.1:g.16366C=
NG_008836.2:g.16366C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1347C= MANE Select	ENSP00000355627.5:p.Arg449=
ENST00000679738.1:c.1347C=	ENSP00000505063.1:p.Arg449=
ENST00000679802.1:c.*806C=	ENSP00000505184.1:n.*806C=
ENST00000679854.1:n.5652C=
ENST00000679957.1:c.1338C=	ENSP00000506646.1:p.Arg446=
ENST00000680041.1:c.1347C=	ENSP00000504866.1:p.Arg449=
ENST00000680783.1:c.829+6770C=	ENSP00000506329.1:n.829+6770C=
ENST00000681269.1:c.1347C=	ENSP00000505985.1:p.Arg449=
ENST00000681347.1:n.3453C=
ENST00000681514.1:c.1347C=	ENSP00000505963.1:p.Arg449=
ENST00000681772.1:c.*841C=	ENSP00000505829.1:n.*841C=
ENST00000366667.4:c.1374C=	ENSP00000355627.4:p.Arg458=
NM_000029.3:c.1374C=	NP_000020.1:p.Arg458=
NM_000029.4:c.1374C=	NP_000020.1:p.Arg458=
NM_001382817.3:c.1347C=	NP_001369746.2:p.Arg449=
NM_001384479.1:c.1347C= MANE Select	NP_001371408.1:p.Arg449=