Canonical Allele Identifier: CA1226667818

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230706089C= , CM000663.2:g.230706089C=	GRCh38
NC_000001.10:g.230841835C= , CM000663.1:g.230841835C=	GRCh37
NC_000001.9:g.228908458C=	NCBI36
NG_008836.1:g.13502G=
NG_008836.2:g.13502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.941G= MANE Select	ENSP00000355627.5:p.Ser314=
ENST00000679684.1:c.941G=	ENSP00000505981.1:p.Ser314=
ENST00000679738.1:c.941G=	ENSP00000505063.1:p.Ser314=
ENST00000679802.1:c.*400G=	ENSP00000505184.1:n.*400G=
ENST00000679854.1:n.5246G=
ENST00000679957.1:c.941G=	ENSP00000506646.1:p.Ser314=
ENST00000680041.1:c.941G=	ENSP00000504866.1:p.Ser314=
ENST00000680783.1:c.829+3906G=	ENSP00000506329.1:n.829+3906G=
ENST00000681269.1:c.941G=	ENSP00000505985.1:p.Ser314=
ENST00000681347.1:n.1452G=
ENST00000681514.1:c.941G=	ENSP00000505963.1:p.Ser314=
ENST00000681772.1:c.941G=	ENSP00000505829.1:p.Ser314=
ENST00000366667.4:c.968G=	ENSP00000355627.4:p.Ser323=
NM_000029.3:c.968G=	NP_000020.1:p.Ser323=
NM_000029.4:c.968G=	NP_000020.1:p.Ser323=
NM_001382817.3:c.941G=	NP_001369746.2:p.Ser314=
NM_001384479.1:c.941G= MANE Select	NP_001371408.1:p.Ser314=