Canonical Allele Identifier: CA1140520116
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702394_230702396delinsAAA , CM000663.2:g.230702394_230702396delinsAAA GRCh38
NC_000001.10:g.230838140_230838142delinsAAA , CM000663.1:g.230838140_230838142delinsAAA GRCh37
NC_000001.9:g.228904763_228904765delinsAAA NCBI36
NG_008836.1:g.17195_17197delinsTTT
NG_008836.2:g.17195_17197delinsTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*745_*747delinsTTT ENSP00000505063.1:n.*745_*747delinsTTT
ENST00000679802.1:c.*1635_*1637delinsTTT ENSP00000505184.1:n.*1635_*1637delinsTTT
ENST00000679854.1:n.6481_6483delinsTTT
ENST00000680041.1:c.*745_*747delinsTTT ENSP00000504866.1:n.*745_*747delinsTTT
ENST00000680783.1:c.829+7599_829+7601delinsTTT ENSP00000506329.1:n.829+7599_829+7601delinsTTT
ENST00000681347.1:n.4282_4284delinsTTT
ENST00000681514.1:c.*745_*747delinsTTT ENSP00000505963.1:n.*745_*747delinsTTT
ENST00000681772.1:c.*1670_*1672delinsTTT ENSP00000505829.1:n.*1670_*1672delinsTTT