Canonical Allele Identifier: CA2650970694

Gene: AGT

Linked Data

• gnomAD v4: 1-230704194-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704199del , CM000663.2:g.230704199del	GRCh38
NC_000001.10:g.230839945del , CM000663.1:g.230839945del	GRCh37
NC_000001.9:g.228906568del	NCBI36
NG_008836.1:g.15396del
NG_008836.2:g.15396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1240del MANE Select	ENSP00000355627.5:p.Glu414ArgfsTer3
ENST00000679684.1:c.1240del	ENSP00000505981.1:p.Glu414ArgfsTer?
ENST00000679738.1:c.1240del	ENSP00000505063.1:p.Glu414ArgfsTer3
ENST00000679802.1:c.*699del	ENSP00000505184.1:n.*699del
ENST00000679854.1:n.5545del
ENST00000679957.1:c.1233+7del	ENSP00000506646.1:n.1233+7del
ENST00000680041.1:c.1240del	ENSP00000504866.1:p.Glu414ArgfsTer3
ENST00000680783.1:c.829+5800del	ENSP00000506329.1:n.829+5800del
ENST00000681269.1:c.1240del	ENSP00000505985.1:p.Glu414ArgfsTer3
ENST00000681347.1:n.3346del
ENST00000681514.1:c.1240del	ENSP00000505963.1:p.Glu414ArgfsTer3
ENST00000681772.1:c.*734del	ENSP00000505829.1:n.*734del
ENST00000366667.4:c.1267del	ENSP00000355627.4:p.Glu423ArgfsTer3
NM_000029.3:c.1267del	NP_000020.1:p.Glu423ArgfsTer3
NM_000029.4:c.1267del	NP_000020.1:p.Glu423ArgfsTer3
NM_001382817.3:c.1240del	NP_001369746.2:p.Glu414ArgfsTer3
NM_001384479.1:c.1240del MANE Select	NP_001371408.1:p.Glu414ArgfsTer3