Canonical Allele Identifier: CA529691726

Gene: AGT

Linked Data

• dbSNP Id: rs1403081602
• gnomAD v2: 1-230849261-ATTAG-A
• MyVariant Identifiers: chr1:g.230849262_230849265del (hg19) ; chr1:g.230713516_230713519del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713518_230713521del , CM000663.2:g.230713518_230713521del	GRCh38
NC_000001.10:g.230849264_230849267del , CM000663.1:g.230849264_230849267del	GRCh37
NC_000001.9:g.228915887_228915890del	NCBI36
NG_008836.1:g.6072_6075del
NG_008836.2:g.6072_6075del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+567_-31+570del MANE Select	ENSP00000355627.5:n.-31+567_-31+570del
ENST00000679684.1:c.-31+567_-31+570del	ENSP00000505981.1:n.-31+567_-31+570del
ENST00000679738.1:c.-31+567_-31+570del	ENSP00000505063.1:n.-31+567_-31+570del
ENST00000679802.1:c.-31+567_-31+570del	ENSP00000505184.1:n.-31+567_-31+570del
ENST00000679854.1:n.481+567_481+570del
ENST00000679957.1:c.-31+567_-31+570del	ENSP00000506646.1:n.-31+567_-31+570del
ENST00000680041.1:c.-156+567_-156+570del	ENSP00000504866.1:n.-156+567_-156+570del
ENST00000680783.1:c.-31+567_-31+570del	ENSP00000506329.1:n.-31+567_-31+570del
ENST00000681269.1:c.-30-2666_-30-2663del	ENSP00000505985.1:n.-30-2666_-30-2663del
ENST00000681347.1:n.481+567_481+570del
ENST00000681514.1:c.-117-150_-117-147del	ENSP00000505963.1:n.-117-150_-117-147del
ENST00000681772.1:c.-31+567_-31+570del	ENSP00000505829.1:n.-31+567_-31+570del
ENST00000366667.4:c.-4+567_-4+570del	ENSP00000355627.4:n.-4+567_-4+570del
NM_000029.3:c.-4+567_-4+570del	NP_000020.1:n.-4+567_-4+570del
NM_000029.4:c.-4+567_-4+570del	NP_000020.1:n.-4+567_-4+570del
NM_001382817.3:c.-30-2666_-30-2663del	NP_001369746.2:n.-30-2666_-30-2663del
NM_001384479.1:c.-31+567_-31+570del MANE Select	NP_001371408.1:n.-31+567_-31+570del