Canonical Allele Identifier: CA1226666646

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703321G= , CM000663.2:g.230703321G=	GRCh38
NC_000001.10:g.230839067G= , CM000663.1:g.230839067G=	GRCh37
NC_000001.9:g.228905690G=	NCBI36
NG_008836.1:g.16270C=
NG_008836.2:g.16270C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1251C= MANE Select	ENSP00000355627.5:p.Asn417=
ENST00000679738.1:c.1251C=	ENSP00000505063.1:p.Asn417=
ENST00000679802.1:c.*710C=	ENSP00000505184.1:n.*710C=
ENST00000679854.1:n.5556C=
ENST00000679957.1:c.1242C=	ENSP00000506646.1:p.Asn414=
ENST00000680041.1:c.1251C=	ENSP00000504866.1:p.Asn417=
ENST00000680783.1:c.829+6674C=	ENSP00000506329.1:n.829+6674C=
ENST00000681269.1:c.1251C=	ENSP00000505985.1:p.Asn417=
ENST00000681347.1:n.3357C=
ENST00000681514.1:c.1251C=	ENSP00000505963.1:p.Asn417=
ENST00000681772.1:c.*745C=	ENSP00000505829.1:n.*745C=
ENST00000366667.4:c.1278C=	ENSP00000355627.4:p.Asn426=
NM_000029.3:c.1278C=	NP_000020.1:p.Asn426=
NM_000029.4:c.1278C=	NP_000020.1:p.Asn426=
NM_001382817.3:c.1251C=	NP_001369746.2:p.Asn417=
NM_001384479.1:c.1251C= MANE Select	NP_001371408.1:p.Asn417=