Canonical Allele Identifier: CA1226667649

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705685_230705686delinsAG , CM000663.2:g.230705685_230705686delinsAG	GRCh38
NC_000001.10:g.230841431_230841432delinsAG , CM000663.1:g.230841431_230841432delinsAG	GRCh37
NC_000001.9:g.228908054_228908055delinsAG	NCBI36
NG_008836.1:g.13905_13906delinsCT
NG_008836.2:g.13905_13906delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1097+247_1097+248delinsCT MANE Select	ENSP00000355627.5:n.1097+247_1097+248delinsCT
ENST00000679684.1:c.1097+247_1097+248delinsCT	ENSP00000505981.1:n.1097+247_1097+248delinsCT
ENST00000679738.1:c.1097+247_1097+248delinsCT	ENSP00000505063.1:n.1097+247_1097+248delinsCT
ENST00000679802.1:c.*556+247_*556+248delinsCT	ENSP00000505184.1:n.*556+247_*556+248delinsCT
ENST00000679854.1:n.5402+247_5402+248delinsCT
ENST00000679957.1:c.1097+247_1097+248delinsCT	ENSP00000506646.1:n.1097+247_1097+248delinsCT
ENST00000680041.1:c.1097+247_1097+248delinsCT	ENSP00000504866.1:n.1097+247_1097+248delinsCT
ENST00000680783.1:c.829+4309_829+4310delinsCT	ENSP00000506329.1:n.829+4309_829+4310delinsCT
ENST00000681269.1:c.1097+247_1097+248delinsCT	ENSP00000505985.1:n.1097+247_1097+248delinsCT
ENST00000681347.1:n.1855_1856delinsCT
ENST00000681514.1:c.1097+247_1097+248delinsCT	ENSP00000505963.1:n.1097+247_1097+248delinsCT
ENST00000681772.1:c.*243_*244delinsCT	ENSP00000505829.1:n.*243_*244delinsCT
ENST00000366667.4:c.1124+247_1124+248delinsCT	ENSP00000355627.4:n.1124+247_1124+248delinsCT
NM_000029.3:c.1124+247_1124+248delinsCT	NP_000020.1:n.1124+247_1124+248delinsCT
NM_000029.4:c.1124+247_1124+248delinsCT	NP_000020.1:n.1124+247_1124+248delinsCT
NM_001382817.3:c.1097+247_1097+248delinsCT	NP_001369746.2:n.1097+247_1097+248delinsCT
NM_001384479.1:c.1097+247_1097+248delinsCT MANE Select	NP_001371408.1:n.1097+247_1097+248delinsCT