Canonical Allele Identifier: CA38874885

Gene: AGT

Linked Data

• dbSNP Id: rs773218571
• MyVariant Identifiers: chr1:g.230849376_230849377del (hg19) ; chr1:g.230713630_230713631del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713635_230713636del , CM000663.2:g.230713635_230713636del	GRCh38
NC_000001.10:g.230849381_230849382del , CM000663.1:g.230849381_230849382del	GRCh37
NC_000001.9:g.228916004_228916005del	NCBI36
NG_008836.1:g.5960_5961del
NG_008836.2:g.5960_5961del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+455_-31+456del MANE Select	ENSP00000355627.5:n.-31+455_-31+456del
ENST00000679684.1:c.-31+455_-31+456del	ENSP00000505981.1:n.-31+455_-31+456del
ENST00000679738.1:c.-31+455_-31+456del	ENSP00000505063.1:n.-31+455_-31+456del
ENST00000679802.1:c.-31+455_-31+456del	ENSP00000505184.1:n.-31+455_-31+456del
ENST00000679854.1:n.481+455_481+456del
ENST00000679957.1:c.-31+455_-31+456del	ENSP00000506646.1:n.-31+455_-31+456del
ENST00000680041.1:c.-156+455_-156+456del	ENSP00000504866.1:n.-156+455_-156+456del
ENST00000680783.1:c.-31+455_-31+456del	ENSP00000506329.1:n.-31+455_-31+456del
ENST00000681269.1:c.-30-2778_-30-2777del	ENSP00000505985.1:n.-30-2778_-30-2777del
ENST00000681347.1:n.481+455_481+456del
ENST00000681514.1:c.-117-262_-117-261del	ENSP00000505963.1:n.-117-262_-117-261del
ENST00000681772.1:c.-31+455_-31+456del	ENSP00000505829.1:n.-31+455_-31+456del
ENST00000366667.4:c.-4+455_-4+456del	ENSP00000355627.4:n.-4+455_-4+456del
NM_000029.3:c.-4+455_-4+456del	NP_000020.1:n.-4+455_-4+456del
NM_000029.4:c.-4+455_-4+456del	NP_000020.1:n.-4+455_-4+456del
NM_001382817.3:c.-30-2778_-30-2777del	NP_001369746.2:n.-30-2778_-30-2777del
NM_001384479.1:c.-31+455_-31+456del MANE Select	NP_001371408.1:n.-31+455_-31+456del