Canonical Allele Identifier: CA1226661604
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230713503_230713504delinsCT , CM000663.2:g.230713503_230713504delinsCT GRCh38
NC_000001.10:g.230849249_230849250delinsCT , CM000663.1:g.230849249_230849250delinsCT GRCh37
NC_000001.9:g.228915872_228915873delinsCT NCBI36
NG_008836.1:g.6087_6088delinsAG
NG_008836.2:g.6087_6088delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.-31+582_-31+583delinsAG MANE Select ENSP00000355627.5:n.-31+582_-31+583delins...
ENST00000679684.1:c.-31+582_-31+583delinsAG ENSP00000505981.1:n.-31+582_-31+583delins...
ENST00000679738.1:c.-31+582_-31+583delinsAG ENSP00000505063.1:n.-31+582_-31+583delins...
ENST00000679802.1:c.-31+582_-31+583delinsAG ENSP00000505184.1:n.-31+582_-31+583delins...
ENST00000679854.1:n.481+582_481+583delinsAG
ENST00000679957.1:c.-31+582_-31+583delinsAG ENSP00000506646.1:n.-31+582_-31+583delins...
ENST00000680041.1:c.-156+582_-156+583delinsAG ENSP00000504866.1:n.-156+582_-156+583deli...
ENST00000680783.1:c.-31+582_-31+583delinsAG ENSP00000506329.1:n.-31+582_-31+583delins...
ENST00000681269.1:c.-30-2651_-30-2650delinsAG ENSP00000505985.1:n.-30-2651_-30-2650deli...
ENST00000681347.1:n.481+582_481+583delinsAG
ENST00000681514.1:c.-117-135_-117-134delinsAG ENSP00000505963.1:n.-117-135_-117-134deli...
ENST00000681772.1:c.-31+582_-31+583delinsAG ENSP00000505829.1:n.-31+582_-31+583delins...
ENST00000366667.4:c.-4+582_-4+583delinsAG ENSP00000355627.4:n.-4+582_-4+583delinsAG...
NM_000029.3:c.-4+582_-4+583delinsAG NP_000020.1:n.-4+582_-4+583delinsAG
NM_000029.4:c.-4+582_-4+583delinsAG NP_000020.1:n.-4+582_-4+583delinsAG
NM_001382817.3:c.-30-2651_-30-2650delinsAG NP_001369746.2:n.-30-2651_-30-2650delinsA...
NM_001384479.1:c.-31+582_-31+583delinsAG MANE Select NP_001371408.1:n.-31+582_-31+583delinsAG