Canonical Allele Identifier: CA1226661534

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713395A= , CM000663.2:g.230713395A=	GRCh38
NC_000001.10:g.230849141A= , CM000663.1:g.230849141A=	GRCh37
NC_000001.9:g.228915764A=	NCBI36
NG_008836.1:g.6196T=
NG_008836.2:g.6196T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.-31+691T= MANE Select	ENSP00000355627.5:n.-31+691T=
ENST00000679684.1:c.-31+691T=	ENSP00000505981.1:n.-31+691T=
ENST00000679738.1:c.-31+691T=	ENSP00000505063.1:n.-31+691T=
ENST00000679802.1:c.-31+691T=	ENSP00000505184.1:n.-31+691T=
ENST00000679854.1:n.481+691T=
ENST00000679957.1:c.-31+691T=	ENSP00000506646.1:n.-31+691T=
ENST00000680041.1:c.-156+691T=	ENSP00000504866.1:n.-156+691T=
ENST00000680783.1:c.-31+691T=	ENSP00000506329.1:n.-31+691T=
ENST00000681269.1:c.-30-2542T=	ENSP00000505985.1:n.-30-2542T=
ENST00000681347.1:n.481+691T=
ENST00000681514.1:c.-117-26T=	ENSP00000505963.1:n.-117-26T=
ENST00000681772.1:c.-31+691T=	ENSP00000505829.1:n.-31+691T=
ENST00000366667.4:c.-4+691T=	ENSP00000355627.4:n.-4+691T=
NM_000029.3:c.-4+691T=	NP_000020.1:n.-4+691T=
NM_000029.4:c.-4+691T=	NP_000020.1:n.-4+691T=
NM_001382817.3:c.-30-2542T=	NP_001369746.2:n.-30-2542T=
NM_001384479.1:c.-31+691T= MANE Select	NP_001371408.1:n.-31+691T=