Canonical Allele Identifier: CA1226669776

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710540_230710541delinsGC , CM000663.2:g.230710540_230710541delinsGC	GRCh38
NC_000001.10:g.230846286_230846287delinsGC , CM000663.1:g.230846286_230846287delinsGC	GRCh37
NC_000001.9:g.228912909_228912910delinsGC	NCBI36
NG_008836.1:g.9050_9051delinsGC
NG_008836.2:g.9050_9051delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.283_284delinsGC MANE Select	ENSP00000355627.5:p.Ala95=
ENST00000679684.1:c.283_284delinsGC	ENSP00000505981.1:p.Ala95=
ENST00000679738.1:c.283_284delinsGC	ENSP00000505063.1:p.Ala95=
ENST00000679802.1:c.283_284delinsGC	ENSP00000505184.1:p.Ala95=
ENST00000679854.1:n.794_795delinsGC
ENST00000679957.1:c.283_284delinsGC	ENSP00000506646.1:p.Ala95=
ENST00000680041.1:c.283_284delinsGC	ENSP00000504866.1:p.Ala95=
ENST00000680783.1:c.283_284delinsGC	ENSP00000506329.1:p.Ala95=
ENST00000681269.1:c.283_284delinsGC	ENSP00000505985.1:p.Ala95=
ENST00000681347.1:n.794_795delinsGC
ENST00000681514.1:c.283_284delinsGC	ENSP00000505963.1:p.Ala95=
ENST00000681772.1:c.283_284delinsGC	ENSP00000505829.1:p.Ala95=
ENST00000366667.4:c.310_311delinsGC	ENSP00000355627.4:p.Ala104=
NM_000029.3:c.310_311delinsGC	NP_000020.1:p.Ala104=
NM_000029.4:c.310_311delinsGC	NP_000020.1:p.Ala104=
NM_001382817.3:c.283_284delinsGC	NP_001369746.2:p.Ala95=
NM_001384479.1:c.283_284delinsGC MANE Select	NP_001371408.1:p.Ala95=