Canonical Allele Identifier: CA38871225
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs141900991
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710043_230710044delinsAC , CM000663.2:g.230710043_230710044delinsAC GRCh38
NC_000001.10:g.230845789_230845790delinsAC , CM000663.1:g.230845789_230845790delinsAC GRCh37
NC_000001.9:g.228912412_228912413delinsAC NCBI36
NG_008836.1:g.9547_9548delinsGT
NG_008836.2:g.9547_9548delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.780_781delinsGT MANE Select ENSP00000355627.5:p.Ala261Ser
ENST00000679684.1:c.780_781delinsGT ENSP00000505981.1:p.Ala261Ser
ENST00000679738.1:c.780_781delinsGT ENSP00000505063.1:p.Ala261Ser
ENST00000679802.1:c.780_781delinsGT ENSP00000505184.1:p.Ala261Ser
ENST00000679854.1:n.1291_1292delinsGT
ENST00000679957.1:c.780_781delinsGT ENSP00000506646.1:p.Ala261Ser
ENST00000680041.1:c.780_781delinsGT ENSP00000504866.1:p.Ala261Ser
ENST00000680783.1:c.780_781delinsGT ENSP00000506329.1:p.Ala261Ser
ENST00000681269.1:c.780_781delinsGT ENSP00000505985.1:p.Ala261Ser
ENST00000681347.1:n.1291_1292delinsGT
ENST00000681514.1:c.780_781delinsGT ENSP00000505963.1:p.Ala261Ser
ENST00000681772.1:c.780_781delinsGT ENSP00000505829.1:p.Ala261Ser
ENST00000366667.4:c.807_808delinsGT ENSP00000355627.4:p.Ala270Ser
NM_000029.3:c.807_808delinsGT NP_000020.1:p.Ala270Ser
NM_000029.4:c.807_808delinsGT NP_000020.1:p.Ala270Ser
NM_001382817.3:c.780_781delinsGT NP_001369746.2:p.Ala261Ser
NM_001384479.1:c.780_781delinsGT MANE Select NP_001371408.1:p.Ala261Ser
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