Canonical Allele Identifier: CA1140726480

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704201C= , CM000663.2:g.230704201C=	GRCh38
NC_000001.10:g.230839947C= , CM000663.1:g.230839947C=	GRCh37
NC_000001.9:g.228906570C=	NCBI36
NG_008836.1:g.15390G=
NG_008836.2:g.15390G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1234G= MANE Select	ENSP00000355627.5:p.Val412=
ENST00000679684.1:c.1234G=	ENSP00000505981.1:p.Val412=
ENST00000679738.1:c.1234G=	ENSP00000505063.1:p.Val412=
ENST00000679802.1:c.*693G=	ENSP00000505184.1:n.*693G=
ENST00000679854.1:n.5539G=
ENST00000679957.1:c.1233+1G=	ENSP00000506646.1:n.1233+1G=
ENST00000680041.1:c.1234G=	ENSP00000504866.1:p.Val412=
ENST00000680783.1:c.829+5794G=	ENSP00000506329.1:n.829+5794G=
ENST00000681269.1:c.1234G=	ENSP00000505985.1:p.Val412=
ENST00000681347.1:n.3340G=
ENST00000681514.1:c.1234G=	ENSP00000505963.1:p.Val412=
ENST00000681772.1:c.*728G=	ENSP00000505829.1:n.*728G=
ENST00000366667.4:c.1261G=	ENSP00000355627.4:p.Val421=
NM_000029.3:c.1261G=	NP_000020.1:p.Val421=
NM_000029.4:c.1261G=	NP_000020.1:p.Val421=
NM_001382817.3:c.1234G=	NP_001369746.2:p.Val412=
NM_001384479.1:c.1234G= MANE Select	NP_001371408.1:p.Val412=