Canonical Allele Identifier: CA1226661972

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714031_230714032delinsAG , CM000663.2:g.230714031_230714032delinsAG	GRCh38
NC_000001.10:g.230849777_230849778delinsAG , CM000663.1:g.230849777_230849778delinsAG	GRCh37
NC_000001.9:g.228916400_228916401delinsAG	NCBI36
NG_008836.1:g.5559_5560delinsCT
NG_008836.2:g.5559_5560delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.-31+54_-31+55delinsCT MANE Select	ENSP00000355627.5:n.-31+54_-31+55delinsCT
ENST00000679684.1:c.-31+54_-31+55delinsCT	ENSP00000505981.1:n.-31+54_-31+55delinsCT
ENST00000679738.1:c.-31+54_-31+55delinsCT	ENSP00000505063.1:n.-31+54_-31+55delinsCT
ENST00000679802.1:c.-31+54_-31+55delinsCT	ENSP00000505184.1:n.-31+54_-31+55delinsCT
ENST00000679854.1:n.481+54_481+55delinsCT
ENST00000679957.1:c.-31+54_-31+55delinsCT	ENSP00000506646.1:n.-31+54_-31+55delinsCT
ENST00000680041.1:c.-156+54_-156+55delinsCT	ENSP00000504866.1:n.-156+54_-156+55delinsCT
ENST00000680783.1:c.-31+54_-31+55delinsCT	ENSP00000506329.1:n.-31+54_-31+55delinsCT
ENST00000681269.1:c.-30-3179_-30-3178delinsCT	ENSP00000505985.1:n.-30-3179_-30-3178delinsCT
ENST00000681347.1:n.481+54_481+55delinsCT
ENST00000681514.1:c.-118+54_-118+55delinsCT	ENSP00000505963.1:n.-118+54_-118+55delinsCT
ENST00000681772.1:c.-31+54_-31+55delinsCT	ENSP00000505829.1:n.-31+54_-31+55delinsCT
ENST00000366667.4:c.-4+54_-4+55delinsCT	ENSP00000355627.4:n.-4+54_-4+55delinsCT
NM_000029.3:c.-4+54_-4+55delinsCT	NP_000020.1:n.-4+54_-4+55delinsCT
NM_000029.4:c.-4+54_-4+55delinsCT	NP_000020.1:n.-4+54_-4+55delinsCT
NM_001382817.3:c.-30-3179_-30-3178delinsCT	NP_001369746.2:n.-30-3179_-30-3178delinsCT
NM_001384479.1:c.-31+54_-31+55delinsCT MANE Select	NP_001371408.1:n.-31+54_-31+55delinsCT