Canonical Allele Identifier: CA1226666654
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230703344_230703347delinsACAT , CM000663.2:g.230703344_230703347delinsACAT GRCh38
NC_000001.10:g.230839090_230839093delinsACAT , CM000663.1:g.230839090_230839093delinsACAT GRCh37
NC_000001.9:g.228905713_228905716delinsACAT NCBI36
NG_008836.1:g.16244_16247delinsATGT
NG_008836.2:g.16244_16247delinsATGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.1243-18_1243-15delinsATGT MANE Select ENSP00000355627.5:n.1243-18_1243-15delinsATGT
ENST00000679738.1:c.1243-18_1243-15delinsATGT ENSP00000505063.1:n.1243-18_1243-15delinsATGT
ENST00000679802.1:c.*702-18_*702-15delinsATGT ENSP00000505184.1:n.*702-18_*702-15delinsATGT
ENST00000679854.1:n.5548-18_5548-15delinsATGT
ENST00000679957.1:c.1234-18_1234-15delinsATGT ENSP00000506646.1:n.1234-18_1234-15delinsATGT
ENST00000680041.1:c.1243-18_1243-15delinsATGT ENSP00000504866.1:n.1243-18_1243-15delinsATGT
ENST00000680783.1:c.829+6648_829+6651delinsATGT ENSP00000506329.1:n.829+6648_829+6651delinsATGT
ENST00000681269.1:c.1243-18_1243-15delinsATGT ENSP00000505985.1:n.1243-18_1243-15delinsATGT
ENST00000681347.1:n.3349-18_3349-15delinsATGT
ENST00000681514.1:c.1243-18_1243-15delinsATGT ENSP00000505963.1:n.1243-18_1243-15delinsATGT
ENST00000681772.1:c.*737-18_*737-15delinsATGT ENSP00000505829.1:n.*737-18_*737-15delinsATGT
ENST00000366667.4:c.1270-18_1270-15delinsATGT ENSP00000355627.4:n.1270-18_1270-15delinsATGT
NM_000029.3:c.1270-18_1270-15delinsATGT NP_000020.1:n.1270-18_1270-15delinsATGT
NM_000029.4:c.1270-18_1270-15delinsATGT NP_000020.1:n.1270-18_1270-15delinsATGT
NM_001382817.3:c.1243-18_1243-15delinsATGT NP_001369746.2:n.1243-18_1243-15delinsATGT
NM_001384479.1:c.1243-18_1243-15delinsATGT MANE Select NP_001371408.1:n.1243-18_1243-15delinsATGT