Canonical Allele Identifier: CA645521368
Gene: AGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230706124_230706125delinsAA , CM000663.2:g.230706124_230706125delinsAA GRCh38
NC_000001.10:g.230841870_230841871delinsAA , CM000663.1:g.230841870_230841871delinsAA GRCh37
NC_000001.9:g.228908493_228908494delinsAA NCBI36
NG_008836.1:g.13466_13467delinsTT
NG_008836.2:g.13466_13467delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.905_906delinsTT MANE Select ENSP00000355627.5:p.Pro302Leu
ENST00000679684.1:c.905_906delinsTT ENSP00000505981.1:p.Pro302Leu
ENST00000679738.1:c.905_906delinsTT ENSP00000505063.1:p.Pro302Leu
ENST00000679802.1:c.*364_*365delinsTT ENSP00000505184.1:n.*364_*365delinsTT
ENST00000679854.1:n.5210_5211delinsTT
ENST00000679957.1:c.905_906delinsTT ENSP00000506646.1:p.Pro302Leu
ENST00000680041.1:c.905_906delinsTT ENSP00000504866.1:p.Pro302Leu
ENST00000680783.1:c.829+3870_829+3871delinsTT ENSP00000506329.1:n.829+3870_829+3871delinsTT
ENST00000681269.1:c.905_906delinsTT ENSP00000505985.1:p.Pro302Leu
ENST00000681347.1:n.1416_1417delinsTT
ENST00000681514.1:c.905_906delinsTT ENSP00000505963.1:p.Pro302Leu
ENST00000681772.1:c.905_906delinsTT ENSP00000505829.1:p.Pro302Leu
ENST00000366667.4:c.932_933delinsTT ENSP00000355627.4:p.Pro311Leu
NM_000029.3:c.932_933delinsTT NP_000020.1:p.Pro311Leu
NM_000029.4:c.932_933delinsTT NP_000020.1:p.Pro311Leu
NM_001382817.3:c.905_906delinsTT NP_001369746.2:p.Pro302Leu
NM_001384479.1:c.905_906delinsTT MANE Select NP_001371408.1:p.Pro302Leu