Canonical Allele Identifier: CA2650971162

Gene: AGT

Linked Data

• gnomAD v4: 1-230703206-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703207del , CM000663.2:g.230703207del	GRCh38
NC_000001.10:g.230838953del , CM000663.1:g.230838953del	GRCh37
NC_000001.9:g.228905576del	NCBI36
NG_008836.1:g.16384del
NG_008836.2:g.16384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1365del MANE Select	ENSP00000355627.5:p.Tyr456MetfsTer18
ENST00000679738.1:c.1365del	ENSP00000505063.1:p.Tyr456MetfsTer18
ENST00000679802.1:c.*824del	ENSP00000505184.1:n.*824del
ENST00000679854.1:n.5670del
ENST00000679957.1:c.1356del	ENSP00000506646.1:p.Tyr453MetfsTer18
ENST00000680041.1:c.1365del	ENSP00000504866.1:p.Tyr456MetfsTer18
ENST00000680783.1:c.829+6788del	ENSP00000506329.1:n.829+6788del
ENST00000681269.1:c.1365del	ENSP00000505985.1:p.Tyr456MetfsTer18
ENST00000681347.1:n.3471del
ENST00000681514.1:c.1365del	ENSP00000505963.1:p.Tyr456MetfsTer18
ENST00000681772.1:c.*859del	ENSP00000505829.1:n.*859del
ENST00000366667.4:c.1392del	ENSP00000355627.4:p.Tyr465MetfsTer18
NM_000029.3:c.1392del	NP_000020.1:p.Tyr465MetfsTer18
NM_000029.4:c.1392del	NP_000020.1:p.Tyr465MetfsTer18
NM_001382817.3:c.1365del	NP_001369746.2:p.Tyr456MetfsTer18
NM_001384479.1:c.1365del MANE Select	NP_001371408.1:p.Tyr456MetfsTer18