Canonical Allele Identifier: CA1226666644

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703317T= , CM000663.2:g.230703317T=	GRCh38
NC_000001.10:g.230839063T= , CM000663.1:g.230839063T=	GRCh37
NC_000001.9:g.228905686T=	NCBI36
NG_008836.1:g.16274A=
NG_008836.2:g.16274A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1255A= MANE Select	ENSP00000355627.5:p.Ile419=
ENST00000679738.1:c.1255A=	ENSP00000505063.1:p.Ile419=
ENST00000679802.1:c.*714A=	ENSP00000505184.1:n.*714A=
ENST00000679854.1:n.5560A=
ENST00000679957.1:c.1246A=	ENSP00000506646.1:p.Ile416=
ENST00000680041.1:c.1255A=	ENSP00000504866.1:p.Ile419=
ENST00000680783.1:c.829+6678A=	ENSP00000506329.1:n.829+6678A=
ENST00000681269.1:c.1255A=	ENSP00000505985.1:p.Ile419=
ENST00000681347.1:n.3361A=
ENST00000681514.1:c.1255A=	ENSP00000505963.1:p.Ile419=
ENST00000681772.1:c.*749A=	ENSP00000505829.1:n.*749A=
ENST00000366667.4:c.1282A=	ENSP00000355627.4:p.Ile428=
NM_000029.3:c.1282A=	NP_000020.1:p.Ile428=
NM_000029.4:c.1282A=	NP_000020.1:p.Ile428=
NM_001382817.3:c.1255A=	NP_001369746.2:p.Ile419=
NM_001384479.1:c.1255A= MANE Select	NP_001371408.1:p.Ile419=