Canonical Allele Identifier: CA1226667078
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704338_230704339delinsCT , CM000663.2:g.230704338_230704339delinsCT GRCh38
NC_000001.10:g.230840084_230840085delinsCT , CM000663.1:g.230840084_230840085delinsCT GRCh37
NC_000001.9:g.228906707_228906708delinsCT NCBI36
NG_008836.1:g.15252_15253delinsAG
NG_008836.2:g.15252_15253delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.1098-2_1098-1delinsAG MANE Select ENSP00000355627.5:n.1098-2_1098-1delinsAG
ENST00000679684.1:c.1098-2_1098-1delinsAG ENSP00000505981.1:n.1098-2_1098-1delinsAG
ENST00000679738.1:c.1098-2_1098-1delinsAG ENSP00000505063.1:n.1098-2_1098-1delinsAG
ENST00000679802.1:c.*557-2_*557-1delinsAG ENSP00000505184.1:n.*557-2_*557-1delinsAG
ENST00000679854.1:n.5403-2_5403-1delinsAG
ENST00000679957.1:c.1098-2_1098-1delinsAG ENSP00000506646.1:n.1098-2_1098-1delinsAG
ENST00000680041.1:c.1098-2_1098-1delinsAG ENSP00000504866.1:n.1098-2_1098-1delinsAG
ENST00000680783.1:c.829+5656_829+5657delinsAG ENSP00000506329.1:n.829+5656_829+5657delinsAG
ENST00000681269.1:c.1098-2_1098-1delinsAG ENSP00000505985.1:n.1098-2_1098-1delinsAG
ENST00000681347.1:n.3202_3203delinsAG
ENST00000681514.1:c.1098-2_1098-1delinsAG ENSP00000505963.1:n.1098-2_1098-1delinsAG
ENST00000681772.1:c.*592-2_*592-1delinsAG ENSP00000505829.1:n.*592-2_*592-1delinsAG
ENST00000366667.4:c.1125-2_1125-1delinsAG ENSP00000355627.4:n.1125-2_1125-1delinsAG
NM_000029.3:c.1125-2_1125-1delinsAG NP_000020.1:n.1125-2_1125-1delinsAG
NM_000029.4:c.1125-2_1125-1delinsAG NP_000020.1:n.1125-2_1125-1delinsAG
NM_001382817.3:c.1098-2_1098-1delinsAG NP_001369746.2:n.1098-2_1098-1delinsAG
NM_001384479.1:c.1098-2_1098-1delinsAG MANE Select NP_001371408.1:n.1098-2_1098-1delinsAG