Canonical Allele Identifier: CA1226667031
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704189A= , CM000663.2:g.230704189A= GRCh38
NC_000001.10:g.230839935A= , CM000663.1:g.230839935A= GRCh37
NC_000001.9:g.228906558A= NCBI36
NG_008836.1:g.15402T=
NG_008836.2:g.15402T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.1242+4T= MANE Select ENSP00000355627.5:n.1242+4T=
ENST00000679684.1:c.1242+4T= ENSP00000505981.1:n.1242+4T=
ENST00000679738.1:c.1242+4T= ENSP00000505063.1:n.1242+4T=
ENST00000679802.1:c.*701+4T= ENSP00000505184.1:n.*701+4T=
ENST00000679854.1:n.5547+4T=
ENST00000679957.1:c.1233+13T= ENSP00000506646.1:n.1233+13T=
ENST00000680041.1:c.1242+4T= ENSP00000504866.1:n.1242+4T=
ENST00000680783.1:c.829+5806T= ENSP00000506329.1:n.829+5806T=
ENST00000681269.1:c.1242+4T= ENSP00000505985.1:n.1242+4T=
ENST00000681347.1:n.3348+4T=
ENST00000681514.1:c.1242+4T= ENSP00000505963.1:n.1242+4T=
ENST00000681772.1:c.*736+4T= ENSP00000505829.1:n.*736+4T=
ENST00000366667.4:c.1269+4T= ENSP00000355627.4:n.1269+4T=
NM_000029.3:c.1269+4T= NP_000020.1:n.1269+4T=
NM_000029.4:c.1269+4T= NP_000020.1:n.1269+4T=
NM_001382817.3:c.1242+4T= NP_001369746.2:n.1242+4T=
NM_001384479.1:c.1242+4T= MANE Select NP_001371408.1:n.1242+4T=