Canonical Allele Identifier: CA1226666378

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702549G= , CM000663.2:g.230702549G=	GRCh38
NC_000001.10:g.230838295G= , CM000663.1:g.230838295G=	GRCh37
NC_000001.9:g.228904918G=	NCBI36
NG_008836.1:g.17042C=
NG_008836.2:g.17042C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*592C= MANE Select	ENSP00000355627.5:n.*592C=
ENST00000679738.1:c.*592C=	ENSP00000505063.1:n.*592C=
ENST00000679802.1:c.*1482C=	ENSP00000505184.1:n.*1482C=
ENST00000679854.1:n.6328C=
ENST00000680041.1:c.*592C=	ENSP00000504866.1:n.*592C=
ENST00000680783.1:c.829+7446C=	ENSP00000506329.1:n.829+7446C=
ENST00000681269.1:c.*592C=	ENSP00000505985.1:n.*592C=
ENST00000681347.1:n.4129C=
ENST00000681514.1:c.*592C=	ENSP00000505963.1:n.*592C=
ENST00000681772.1:c.*1517C=	ENSP00000505829.1:n.*1517C=
ENST00000366667.4:c.*592C=	ENSP00000355627.4:n.*592C=
NM_000029.3:c.*592C=	NP_000020.1:n.*592C=
NM_000029.4:c.*592C=	NP_000020.1:n.*592C=
NM_001382817.3:c.*592C=	NP_001369746.2:n.*592C=
NM_001384479.1:c.*592C= MANE Select	NP_001371408.1:n.*592C=