Canonical Allele Identifier: CA1226666587

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703141T= , CM000663.2:g.230703141T=	GRCh38
NC_000001.10:g.230838887T= , CM000663.1:g.230838887T=	GRCh37
NC_000001.9:g.228905510T=	NCBI36
NG_008836.1:g.16450A=
NG_008836.2:g.16450A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1431A= MANE Select	ENSP00000355627.5:p.Ter477=
ENST00000679738.1:c.1431A=	ENSP00000505063.1:p.Ter477=
ENST00000679802.1:c.*890A=	ENSP00000505184.1:n.*890A=
ENST00000679854.1:n.5736A=
ENST00000679957.1:c.1422A=	ENSP00000506646.1:p.Ter474=
ENST00000680041.1:c.1431A=	ENSP00000504866.1:p.Ter477=
ENST00000680783.1:c.829+6854A=	ENSP00000506329.1:n.829+6854A=
ENST00000681269.1:c.1431A=	ENSP00000505985.1:p.Ter477=
ENST00000681347.1:n.3537A=
ENST00000681514.1:c.1431A=	ENSP00000505963.1:p.Ter477=
ENST00000681772.1:c.*925A=	ENSP00000505829.1:n.*925A=
ENST00000366667.4:c.1458A=	ENSP00000355627.4:p.Ter486=
NM_000029.3:c.1458A=	NP_000020.1:p.Ter486=
NM_000029.4:c.1458A=	NP_000020.1:p.Ter486=
NM_001382817.3:c.1431A=	NP_001369746.2:p.Ter477=
NM_001384479.1:c.1431A= MANE Select	NP_001371408.1:p.Ter477=