Canonical Allele Identifier: CA732698024

Gene: AGT

Linked Data

• dbSNP Id: rs1487692681
• gnomAD v3: 1-230713550-C-CA
• gnomAD v4: 1-230713550-C-CA
• MyVariant Identifiers: chr1:g.230849296_230849297insA (hg19) ; chr1:g.230713550_230713551insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713551dup , CM000663.2:g.230713551dup	GRCh38
NC_000001.10:g.230849297dup , CM000663.1:g.230849297dup	GRCh37
NC_000001.9:g.228915920dup	NCBI36
NG_008836.1:g.6040dup
NG_008836.2:g.6040dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.-31+535dup MANE Select	ENSP00000355627.5:n.-31+535dup
ENST00000679684.1:c.-31+535dup	ENSP00000505981.1:n.-31+535dup
ENST00000679738.1:c.-31+535dup	ENSP00000505063.1:n.-31+535dup
ENST00000679802.1:c.-31+535dup	ENSP00000505184.1:n.-31+535dup
ENST00000679854.1:n.481+535dup
ENST00000679957.1:c.-31+535dup	ENSP00000506646.1:n.-31+535dup
ENST00000680041.1:c.-156+535dup	ENSP00000504866.1:n.-156+535dup
ENST00000680783.1:c.-31+535dup	ENSP00000506329.1:n.-31+535dup
ENST00000681269.1:c.-30-2698dup	ENSP00000505985.1:n.-30-2698dup
ENST00000681347.1:n.481+535dup
ENST00000681514.1:c.-117-182dup	ENSP00000505963.1:n.-117-182dup
ENST00000681772.1:c.-31+535dup	ENSP00000505829.1:n.-31+535dup
ENST00000366667.4:c.-4+535dup	ENSP00000355627.4:n.-4+535dup
NM_000029.3:c.-4+535dup	NP_000020.1:n.-4+535dup
NM_000029.4:c.-4+535dup	NP_000020.1:n.-4+535dup
NM_001382817.3:c.-30-2698dup	NP_001369746.2:n.-30-2698dup
NM_001384479.1:c.-31+535dup MANE Select	NP_001371408.1:n.-31+535dup