Canonical Allele Identifier: CA1226667090
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704357_230704359delinsTTA , CM000663.2:g.230704357_230704359delinsTTA GRCh38
NC_000001.10:g.230840103_230840105delinsTTA , CM000663.1:g.230840103_230840105delinsTTA GRCh37
NC_000001.9:g.228906726_228906728delinsTTA NCBI36
NG_008836.1:g.15232_15234delinsTAA
NG_008836.2:g.15232_15234delinsTAA

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1098-22_1098-20delinsTAA MANE Select ENSP00000355627.5:n.1098-22_1098-20delins...
ENST00000679684.1:c.1098-22_1098-20delinsTAA ENSP00000505981.1:n.1098-22_1098-20delins...
ENST00000679738.1:c.1098-22_1098-20delinsTAA ENSP00000505063.1:n.1098-22_1098-20delins...
ENST00000679802.1:c.*557-22_*557-20delinsTAA ENSP00000505184.1:n.*557-22_*557-20delins...
ENST00000679854.1:n.5403-22_5403-20delinsTAA
ENST00000679957.1:c.1098-22_1098-20delinsTAA ENSP00000506646.1:n.1098-22_1098-20delins...
ENST00000680041.1:c.1098-22_1098-20delinsTAA ENSP00000504866.1:n.1098-22_1098-20delins...
ENST00000680783.1:c.829+5636_829+5638delinsTAA ENSP00000506329.1:n.829+5636_829+5638deli...
ENST00000681269.1:c.1098-22_1098-20delinsTAA ENSP00000505985.1:n.1098-22_1098-20delins...
ENST00000681347.1:n.3182_3184delinsTAA
ENST00000681514.1:c.1098-22_1098-20delinsTAA ENSP00000505963.1:n.1098-22_1098-20delins...
ENST00000681772.1:c.*592-22_*592-20delinsTAA ENSP00000505829.1:n.*592-22_*592-20delins...
ENST00000366667.4:c.1125-22_1125-20delinsTAA ENSP00000355627.4:n.1125-22_1125-20delins...
NM_000029.3:c.1125-22_1125-20delinsTAA NP_000020.1:n.1125-22_1125-20delinsTAA
NM_000029.4:c.1125-22_1125-20delinsTAA NP_000020.1:n.1125-22_1125-20delinsTAA
NM_001382817.3:c.1098-22_1098-20delinsTAA NP_001369746.2:n.1098-22_1098-20delinsTAA...
NM_001384479.1:c.1098-22_1098-20delinsTAA MANE Select NP_001371408.1:n.1098-22_1098-20delinsTAA...