Canonical Allele Identifier: CA529916081

Gene: AGT

Linked Data

• dbSNP Id: rs1558287849
• gnomAD v2: 1-230845896-AC-A
• gnomAD v4: 1-230710150-AC-A
• MyVariant Identifiers: chr1:g.230845897del (hg19) ; chr1:g.230710151del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710152del , CM000663.2:g.230710152del	GRCh38
NC_000001.10:g.230845898del , CM000663.1:g.230845898del	GRCh37
NC_000001.9:g.228912521del	NCBI36
NG_008836.1:g.9440del
NG_008836.2:g.9440del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.673del MANE Select	ENSP00000355627.5:p.Val225SerfsTer25
ENST00000679684.1:c.673del	ENSP00000505981.1:p.Val225SerfsTer25
ENST00000679738.1:c.673del	ENSP00000505063.1:p.Val225SerfsTer25
ENST00000679802.1:c.673del	ENSP00000505184.1:p.Val225SerfsTer25
ENST00000679854.1:n.1184del
ENST00000679957.1:c.673del	ENSP00000506646.1:p.Val225SerfsTer25
ENST00000680041.1:c.673del	ENSP00000504866.1:p.Val225SerfsTer25
ENST00000680783.1:c.673del	ENSP00000506329.1:p.Val225SerfsTer25
ENST00000681269.1:c.673del	ENSP00000505985.1:p.Val225SerfsTer25
ENST00000681347.1:n.1184del
ENST00000681514.1:c.673del	ENSP00000505963.1:p.Val225SerfsTer25
ENST00000681772.1:c.673del	ENSP00000505829.1:p.Val225SerfsTer25
ENST00000366667.4:c.700del	ENSP00000355627.4:p.Val234SerfsTer25
NM_000029.3:c.700del	NP_000020.1:p.Val234SerfsTer25
NM_000029.4:c.700del	NP_000020.1:p.Val234SerfsTer25
NM_001382817.3:c.673del	NP_001369746.2:p.Val225SerfsTer25
NM_001384479.1:c.673del MANE Select	NP_001371408.1:p.Val225SerfsTer25