Canonical Allele Identifier: CA529690821

Gene: AGT

Linked Data

• dbSNP Id: rs1428209294
• gnomAD v2: 1-230839846-AC-A
• gnomAD v3: 1-230704100-AC-A
• gnomAD v4: 1-230704100-AC-A
• MyVariant Identifiers: chr1:g.230839847del (hg19) ; chr1:g.230704101del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704103del , CM000663.2:g.230704103del	GRCh38
NC_000001.10:g.230839849del , CM000663.1:g.230839849del	GRCh37
NC_000001.9:g.228906472del	NCBI36
NG_008836.1:g.15490del
NG_008836.2:g.15490del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1242+92del MANE Select	ENSP00000355627.5:n.1242+92del
ENST00000679684.1:c.1242+92del	ENSP00000505981.1:n.1242+92del
ENST00000679738.1:c.1242+92del	ENSP00000505063.1:n.1242+92del
ENST00000679802.1:c.*701+92del	ENSP00000505184.1:n.*701+92del
ENST00000679854.1:n.5547+92del
ENST00000679957.1:c.1233+101del	ENSP00000506646.1:n.1233+101del
ENST00000680041.1:c.1242+92del	ENSP00000504866.1:n.1242+92del
ENST00000680783.1:c.829+5894del	ENSP00000506329.1:n.829+5894del
ENST00000681269.1:c.1242+92del	ENSP00000505985.1:n.1242+92del
ENST00000681347.1:n.3348+92del
ENST00000681514.1:c.1242+92del	ENSP00000505963.1:n.1242+92del
ENST00000681772.1:c.*736+92del	ENSP00000505829.1:n.*736+92del
ENST00000366667.4:c.1269+92del	ENSP00000355627.4:n.1269+92del
NM_000029.3:c.1269+92del	NP_000020.1:n.1269+92del
NM_000029.4:c.1269+92del	NP_000020.1:n.1269+92del
NM_001382817.3:c.1242+92del	NP_001369746.2:n.1242+92del
NM_001384479.1:c.1242+92del MANE Select	NP_001371408.1:n.1242+92del