Canonical Allele Identifier: CA2607358164

Gene: AGT

Linked Data

• gnomAD v3: 1-230709644-AC-A
• gnomAD v4: 1-230709644-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230709649del , CM000663.2:g.230709649del	GRCh38
NC_000001.10:g.230845395del , CM000663.1:g.230845395del	GRCh37
NC_000001.9:g.228912018del	NCBI36
NG_008836.1:g.9946del
NG_008836.2:g.9946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.829+350del MANE Select	ENSP00000355627.5:n.829+350del
ENST00000679684.1:c.829+350del	ENSP00000505981.1:n.829+350del
ENST00000679738.1:c.829+350del	ENSP00000505063.1:n.829+350del
ENST00000679802.1:c.830-219del	ENSP00000505184.1:n.830-219del
ENST00000679854.1:n.1690del
ENST00000679957.1:c.829+350del	ENSP00000506646.1:n.829+350del
ENST00000680041.1:c.829+350del	ENSP00000504866.1:n.829+350del
ENST00000680783.1:c.829+350del	ENSP00000506329.1:n.829+350del
ENST00000681269.1:c.829+350del	ENSP00000505985.1:n.829+350del
ENST00000681347.1:n.1340+350del
ENST00000681514.1:c.829+350del	ENSP00000505963.1:n.829+350del
ENST00000681772.1:c.829+350del	ENSP00000505829.1:n.829+350del
ENST00000366667.4:c.856+350del	ENSP00000355627.4:n.856+350del
NM_000029.3:c.856+350del	NP_000020.1:n.856+350del
NM_000029.4:c.856+350del	NP_000020.1:n.856+350del
NM_001382817.3:c.829+350del	NP_001369746.2:n.829+350del
NM_001384479.1:c.829+350del MANE Select	NP_001371408.1:n.829+350del