Canonical Allele Identifier: CA2650971419

Gene: AGT

Linked Data

• gnomAD v4: 1-230710757-C-CAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710759_230710760insAAG , CM000663.2:g.230710759_230710760insAAG	GRCh38
NC_000001.10:g.230846505_230846506insAAG , CM000663.1:g.230846505_230846506insAAG	GRCh37
NC_000001.9:g.228913128_228913129insAAG	NCBI36
NG_008836.1:g.8833_8834insTCT
NG_008836.2:g.8833_8834insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.66_67insTCT MANE Select	ENSP00000355627.5:p.Ala22_Ala23insSer
ENST00000679684.1:c.66_67insTCT	ENSP00000505981.1:p.Ala22_Ala23insSer
ENST00000679738.1:c.66_67insTCT	ENSP00000505063.1:p.Ala22_Ala23insSer
ENST00000679802.1:c.66_67insTCT	ENSP00000505184.1:p.Ala22_Ala23insSer
ENST00000679854.1:n.577_578insTCT
ENST00000679957.1:c.66_67insTCT	ENSP00000506646.1:p.Ala22_Ala23insSer
ENST00000680041.1:c.66_67insTCT	ENSP00000504866.1:p.Ala22_Ala23insSer
ENST00000680783.1:c.66_67insTCT	ENSP00000506329.1:p.Ala22_Ala23insSer
ENST00000681269.1:c.66_67insTCT	ENSP00000505985.1:p.Ala22_Ala23insSer
ENST00000681347.1:n.577_578insTCT
ENST00000681514.1:c.66_67insTCT	ENSP00000505963.1:p.Ala22_Ala23insSer
ENST00000681772.1:c.66_67insTCT	ENSP00000505829.1:p.Ala22_Ala23insSer
ENST00000366667.4:c.93_94insTCT	ENSP00000355627.4:p.Ala31_Ala32insSer
NM_000029.3:c.93_94insTCT	NP_000020.1:p.Ala31_Ala32insSer
NM_000029.4:c.93_94insTCT	NP_000020.1:p.Ala31_Ala32insSer
NM_001382817.3:c.66_67insTCT	NP_001369746.2:p.Ala22_Ala23insSer
NM_001384479.1:c.66_67insTCT MANE Select	NP_001371408.1:p.Ala22_Ala23insSer