Canonical Allele Identifier: CA732700759

Gene: AGT

Linked Data

• dbSNP Id: rs1275805226
• gnomAD v3: 1-230706147-TG-T
• gnomAD v4: 1-230706147-TG-T
• MyVariant Identifiers: chr1:g.230841894del (hg19) ; chr1:g.230706148del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230706148del , CM000663.2:g.230706148del	GRCh38
NC_000001.10:g.230841894del , CM000663.1:g.230841894del	GRCh37
NC_000001.9:g.228908517del	NCBI36
NG_008836.1:g.13443del
NG_008836.2:g.13443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.882del MANE Select	ENSP00000355627.5:p.Asp294GlufsTer29
ENST00000679684.1:c.882del	ENSP00000505981.1:p.Asp294GlufsTer29
ENST00000679738.1:c.882del	ENSP00000505063.1:p.Asp294GlufsTer29
ENST00000679802.1:c.*341del	ENSP00000505184.1:n.*341del
ENST00000679854.1:n.5187del
ENST00000679957.1:c.882del	ENSP00000506646.1:p.Asp294GlufsTer29
ENST00000680041.1:c.882del	ENSP00000504866.1:p.Asp294GlufsTer29
ENST00000680783.1:c.829+3847del	ENSP00000506329.1:n.829+3847del
ENST00000681269.1:c.882del	ENSP00000505985.1:p.Asp294GlufsTer29
ENST00000681347.1:n.1393del
ENST00000681514.1:c.882del	ENSP00000505963.1:p.Asp294GlufsTer29
ENST00000681772.1:c.882del	ENSP00000505829.1:p.Asp294GlufsTer29
ENST00000366667.4:c.909del	ENSP00000355627.4:p.Asp303GlufsTer29
NM_000029.3:c.909del	NP_000020.1:p.Asp303GlufsTer29
NM_000029.4:c.909del	NP_000020.1:p.Asp303GlufsTer29
NM_001382817.3:c.882del	NP_001369746.2:p.Asp294GlufsTer29
NM_001384479.1:c.882del MANE Select	NP_001371408.1:p.Asp294GlufsTer29