Canonical Allele Identifier: CA2650971192
Gene: AGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705939_230705940insTTTCTTC , CM000663.2:g.230705939_230705940insTTTCTTC GRCh38
NC_000001.10:g.230841685_230841686insTTTCTTC , CM000663.1:g.230841685_230841686insTTTCTTC GRCh37
NC_000001.9:g.228908308_228908309insTTTCTTC NCBI36
NG_008836.1:g.13651_13652insGAAGAAA
NG_008836.2:g.13651_13652insGAAGAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1090_1091insGAAGAAA MANE Select ENSP00000355627.5:p.Ser364Ter
ENST00000679684.1:c.1090_1091insGAAGAAA ENSP00000505981.1:p.Ser364Ter
ENST00000679738.1:c.1090_1091insGAAGAAA ENSP00000505063.1:p.Ser364Ter
ENST00000679802.1:c.*549_*550insGAAGAAA ENSP00000505184.1:n.*549_*550insGAAGAAA
ENST00000679854.1:n.5395_5396insGAAGAAA
ENST00000679957.1:c.1090_1091insGAAGAAA ENSP00000506646.1:p.Ser364Ter
ENST00000680041.1:c.1090_1091insGAAGAAA ENSP00000504866.1:p.Ser364Ter
ENST00000680783.1:c.829+4055_829+4056insGAAGAAA ENSP00000506329.1:n.829+4055_829+4056insG...
ENST00000681269.1:c.1090_1091insGAAGAAA ENSP00000505985.1:p.Ser364Ter
ENST00000681347.1:n.1601_1602insGAAGAAA
ENST00000681514.1:c.1090_1091insGAAGAAA ENSP00000505963.1:p.Ser364Ter
ENST00000681772.1:c.1090_1091insGAAGAAA ENSP00000505829.1:p.Ser364Ter
ENST00000366667.4:c.1117_1118insGAAGAAA ENSP00000355627.4:p.Ser373Ter
NM_000029.3:c.1117_1118insGAAGAAA NP_000020.1:p.Ser373Ter
NM_000029.4:c.1117_1118insGAAGAAA NP_000020.1:p.Ser373Ter
NM_001382817.3:c.1090_1091insGAAGAAA NP_001369746.2:p.Ser364Ter
NM_001384479.1:c.1090_1091insGAAGAAA MANE Select NP_001371408.1:p.Ser364Ter