Canonical Allele Identifier: CA38870195

Gene: AGT

Linked Data

• dbSNP Id: rs1007548246
• gnomAD v2: 1-230844259-C-CCA
• gnomAD v3: 1-230708513-C-CCA
• gnomAD v4: 1-230708513-C-CCA
• MyVariant Identifiers: chr1:g.230844259_230844260insCA (hg19) ; chr1:g.230708513_230708514insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230708514_230708515dup , CM000663.2:g.230708514_230708515dup	GRCh38
NC_000001.10:g.230844260_230844261dup , CM000663.1:g.230844260_230844261dup	GRCh37
NC_000001.9:g.228910883_228910884dup	NCBI36
NG_008836.1:g.11076_11077dup
NG_008836.2:g.11076_11077dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.829+1480_829+1481dup MANE Select	ENSP00000355627.5:n.829+1480_829+1481dup
ENST00000679684.1:c.829+1480_829+1481dup	ENSP00000505981.1:n.829+1480_829+1481dup
ENST00000679738.1:c.829+1480_829+1481dup	ENSP00000505063.1:n.829+1480_829+1481dup
ENST00000679802.1:c.*288+592_*288+593dup	ENSP00000505184.1:n.*288+592_*288+593dup
ENST00000679854.1:n.2820_2821dup
ENST00000679957.1:c.829+1480_829+1481dup	ENSP00000506646.1:n.829+1480_829+1481dup
ENST00000680041.1:c.829+1480_829+1481dup	ENSP00000504866.1:n.829+1480_829+1481dup
ENST00000680783.1:c.829+1480_829+1481dup	ENSP00000506329.1:n.829+1480_829+1481dup
ENST00000681269.1:c.829+1480_829+1481dup	ENSP00000505985.1:n.829+1480_829+1481dup
ENST00000681347.1:n.1340+1480_1340+1481dup
ENST00000681514.1:c.829+1480_829+1481dup	ENSP00000505963.1:n.829+1480_829+1481dup
ENST00000681772.1:c.829+1480_829+1481dup	ENSP00000505829.1:n.829+1480_829+1481dup
ENST00000366667.4:c.856+1480_856+1481dup	ENSP00000355627.4:n.856+1480_856+1481dup
NM_000029.3:c.856+1480_856+1481dup	NP_000020.1:n.856+1480_856+1481dup
NM_000029.4:c.856+1480_856+1481dup	NP_000020.1:n.856+1480_856+1481dup
NM_001382817.3:c.829+1480_829+1481dup	NP_001369746.2:n.829+1480_829+1481dup
NM_001384479.1:c.829+1480_829+1481dup MANE Select	NP_001371408.1:n.829+1480_829+1481dup