Canonical Allele Identifier: CA1226669569

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710028T= , CM000663.2:g.230710028T=	GRCh38
NC_000001.10:g.230845774T= , CM000663.1:g.230845774T=	GRCh37
NC_000001.9:g.228912397T=	NCBI36
NG_008836.1:g.9563A=
NG_008836.2:g.9563A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.796A= MANE Select	ENSP00000355627.5:p.Thr266=
ENST00000679684.1:c.796A=	ENSP00000505981.1:p.Thr266=
ENST00000679738.1:c.796A=	ENSP00000505063.1:p.Thr266=
ENST00000679802.1:c.796A=	ENSP00000505184.1:p.Thr266=
ENST00000679854.1:n.1307A=
ENST00000679957.1:c.796A=	ENSP00000506646.1:p.Thr266=
ENST00000680041.1:c.796A=	ENSP00000504866.1:p.Thr266=
ENST00000680783.1:c.796A=	ENSP00000506329.1:p.Thr266=
ENST00000681269.1:c.796A=	ENSP00000505985.1:p.Thr266=
ENST00000681347.1:n.1307A=
ENST00000681514.1:c.796A=	ENSP00000505963.1:p.Thr266=
ENST00000681772.1:c.796A=	ENSP00000505829.1:p.Thr266=
ENST00000366667.4:c.823A=	ENSP00000355627.4:p.Thr275=
NM_000029.3:c.823A=	NP_000020.1:p.Thr275=
NM_000029.4:c.823A=	NP_000020.1:p.Thr275=
NM_001382817.3:c.796A=	NP_001369746.2:p.Thr266=
NM_001384479.1:c.796A= MANE Select	NP_001371408.1:p.Thr266=