Canonical Allele Identifier: CA1013240076

Gene: AGT

Linked Data

• dbSNP Id: rs1663565254
• gnomAD v3: 1-230710739-TG-T
• gnomAD v4: 1-230710739-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710740del , CM000663.2:g.230710740del	GRCh38
NC_000001.10:g.230846486del , CM000663.1:g.230846486del	GRCh37
NC_000001.9:g.228913109del	NCBI36
NG_008836.1:g.8851del
NG_008836.2:g.8851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.84del MANE Select	ENSP00000355627.5:p.Tyr28Ter
ENST00000679684.1:c.84del	ENSP00000505981.1:p.Tyr28Ter
ENST00000679738.1:c.84del	ENSP00000505063.1:p.Tyr28Ter
ENST00000679802.1:c.84del	ENSP00000505184.1:p.Tyr28Ter
ENST00000679854.1:n.595del
ENST00000679957.1:c.84del	ENSP00000506646.1:p.Tyr28Ter
ENST00000680041.1:c.84del	ENSP00000504866.1:p.Tyr28Ter
ENST00000680783.1:c.84del	ENSP00000506329.1:p.Tyr28Ter
ENST00000681269.1:c.84del	ENSP00000505985.1:p.Tyr28Ter
ENST00000681347.1:n.595del
ENST00000681514.1:c.84del	ENSP00000505963.1:p.Tyr28Ter
ENST00000681772.1:c.84del	ENSP00000505829.1:p.Tyr28Ter
ENST00000366667.4:c.111del	ENSP00000355627.4:p.Tyr37Ter
NM_000029.3:c.111del	NP_000020.1:p.Tyr37Ter
NM_000029.4:c.111del	NP_000020.1:p.Tyr37Ter
NM_001382817.3:c.84del	NP_001369746.2:p.Tyr28Ter
NM_001384479.1:c.84del MANE Select	NP_001371408.1:p.Tyr28Ter