Canonical Allele Identifier: CA1226661582
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230713467_230713468delinsAT , CM000663.2:g.230713467_230713468delinsAT GRCh38
NC_000001.10:g.230849213_230849214delinsAT , CM000663.1:g.230849213_230849214delinsAT GRCh37
NC_000001.9:g.228915836_228915837delinsAT NCBI36
NG_008836.1:g.6123_6124delinsAT
NG_008836.2:g.6123_6124delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.-31+618_-31+619delinsAT MANE Select ENSP00000355627.5:n.-31+618_-31+619delins...
ENST00000679684.1:c.-31+618_-31+619delinsAT ENSP00000505981.1:n.-31+618_-31+619delins...
ENST00000679738.1:c.-31+618_-31+619delinsAT ENSP00000505063.1:n.-31+618_-31+619delins...
ENST00000679802.1:c.-31+618_-31+619delinsAT ENSP00000505184.1:n.-31+618_-31+619delins...
ENST00000679854.1:n.481+618_481+619delinsAT
ENST00000679957.1:c.-31+618_-31+619delinsAT ENSP00000506646.1:n.-31+618_-31+619delins...
ENST00000680041.1:c.-156+618_-156+619delinsAT ENSP00000504866.1:n.-156+618_-156+619deli...
ENST00000680783.1:c.-31+618_-31+619delinsAT ENSP00000506329.1:n.-31+618_-31+619delins...
ENST00000681269.1:c.-30-2615_-30-2614delinsAT ENSP00000505985.1:n.-30-2615_-30-2614deli...
ENST00000681347.1:n.481+618_481+619delinsAT
ENST00000681514.1:c.-117-99_-117-98delinsAT ENSP00000505963.1:n.-117-99_-117-98delins...
ENST00000681772.1:c.-31+618_-31+619delinsAT ENSP00000505829.1:n.-31+618_-31+619delins...
ENST00000366667.4:c.-4+618_-4+619delinsAT ENSP00000355627.4:n.-4+618_-4+619delinsAT...
NM_000029.3:c.-4+618_-4+619delinsAT NP_000020.1:n.-4+618_-4+619delinsAT
NM_000029.4:c.-4+618_-4+619delinsAT NP_000020.1:n.-4+618_-4+619delinsAT
NM_001382817.3:c.-30-2615_-30-2614delinsAT NP_001369746.2:n.-30-2615_-30-2614delinsA...
NM_001384479.1:c.-31+618_-31+619delinsAT MANE Select NP_001371408.1:n.-31+618_-31+619delinsAT