Canonical Allele Identifier: CA1226661618

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713522C= , CM000663.2:g.230713522C=	GRCh38
NC_000001.10:g.230849268C= , CM000663.1:g.230849268C=	GRCh37
NC_000001.9:g.228915891C=	NCBI36
NG_008836.1:g.6069G=
NG_008836.2:g.6069G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+564G= MANE Select	ENSP00000355627.5:n.-31+564G=
ENST00000679684.1:c.-31+564G=	ENSP00000505981.1:n.-31+564G=
ENST00000679738.1:c.-31+564G=	ENSP00000505063.1:n.-31+564G=
ENST00000679802.1:c.-31+564G=	ENSP00000505184.1:n.-31+564G=
ENST00000679854.1:n.481+564G=
ENST00000679957.1:c.-31+564G=	ENSP00000506646.1:n.-31+564G=
ENST00000680041.1:c.-156+564G=	ENSP00000504866.1:n.-156+564G=
ENST00000680783.1:c.-31+564G=	ENSP00000506329.1:n.-31+564G=
ENST00000681269.1:c.-30-2669G=	ENSP00000505985.1:n.-30-2669G=
ENST00000681347.1:n.481+564G=
ENST00000681514.1:c.-117-153G=	ENSP00000505963.1:n.-117-153G=
ENST00000681772.1:c.-31+564G=	ENSP00000505829.1:n.-31+564G=
ENST00000366667.4:c.-4+564G=	ENSP00000355627.4:n.-4+564G=
NM_000029.3:c.-4+564G=	NP_000020.1:n.-4+564G=
NM_000029.4:c.-4+564G=	NP_000020.1:n.-4+564G=
NM_001382817.3:c.-30-2669G=	NP_001369746.2:n.-30-2669G=
NM_001384479.1:c.-31+564G= MANE Select	NP_001371408.1:n.-31+564G=