Canonical Allele Identifier: CA1226666604

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703194_230703195delinsCG , CM000663.2:g.230703194_230703195delinsCG	GRCh38
NC_000001.10:g.230838940_230838941delinsCG , CM000663.1:g.230838940_230838941delinsCG	GRCh37
NC_000001.9:g.228905563_228905564delinsCG	NCBI36
NG_008836.1:g.16396_16397delinsCG
NG_008836.2:g.16396_16397delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1377_1378delinsCG MANE Select	ENSP00000355627.5:p.Ser459=
ENST00000679738.1:c.1377_1378delinsCG	ENSP00000505063.1:p.Ser459=
ENST00000679802.1:c.*836_*837delinsCG	ENSP00000505184.1:n.*836_*837delinsCG
ENST00000679854.1:n.5682_5683delinsCG
ENST00000679957.1:c.1368_1369delinsCG	ENSP00000506646.1:p.Ser456=
ENST00000680041.1:c.1377_1378delinsCG	ENSP00000504866.1:p.Ser459=
ENST00000680783.1:c.829+6800_829+6801delinsCG	ENSP00000506329.1:n.829+6800_829+6801delinsCG
ENST00000681269.1:c.1377_1378delinsCG	ENSP00000505985.1:p.Ser459=
ENST00000681347.1:n.3483_3484delinsCG
ENST00000681514.1:c.1377_1378delinsCG	ENSP00000505963.1:p.Ser459=
ENST00000681772.1:c.*871_*872delinsCG	ENSP00000505829.1:n.*871_*872delinsCG
ENST00000366667.4:c.1404_1405delinsCG	ENSP00000355627.4:p.Ser468=
NM_000029.3:c.1404_1405delinsCG	NP_000020.1:p.Ser468=
NM_000029.4:c.1404_1405delinsCG	NP_000020.1:p.Ser468=
NM_001382817.3:c.1377_1378delinsCG	NP_001369746.2:p.Ser459=
NM_001384479.1:c.1377_1378delinsCG MANE Select	NP_001371408.1:p.Ser459=