Canonical Allele Identifier: CA1226667745
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705874C= , CM000663.2:g.230705874C= GRCh38
NC_000001.10:g.230841620C= , CM000663.1:g.230841620C= GRCh37
NC_000001.9:g.228908243C= NCBI36
NG_008836.1:g.13717G=
NG_008836.2:g.13717G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1097+59G= MANE Select ENSP00000355627.5:n.1097+59G=
ENST00000679684.1:c.1097+59G= ENSP00000505981.1:n.1097+59G=
ENST00000679738.1:c.1097+59G= ENSP00000505063.1:n.1097+59G=
ENST00000679802.1:c.*556+59G= ENSP00000505184.1:n.*556+59G=
ENST00000679854.1:n.5402+59G=
ENST00000679957.1:c.1097+59G= ENSP00000506646.1:n.1097+59G=
ENST00000680041.1:c.1097+59G= ENSP00000504866.1:n.1097+59G=
ENST00000680783.1:c.829+4121G= ENSP00000506329.1:n.829+4121G=
ENST00000681269.1:c.1097+59G= ENSP00000505985.1:n.1097+59G=
ENST00000681347.1:n.1667G=
ENST00000681514.1:c.1097+59G= ENSP00000505963.1:n.1097+59G=
ENST00000681772.1:c.*55G= ENSP00000505829.1:n.*55G=
ENST00000366667.4:c.1124+59G= ENSP00000355627.4:n.1124+59G=
NM_000029.3:c.1124+59G= NP_000020.1:n.1124+59G=
NM_000029.4:c.1124+59G= NP_000020.1:n.1124+59G=
NM_001382817.3:c.1097+59G= NP_001369746.2:n.1097+59G=
NM_001384479.1:c.1097+59G= MANE Select NP_001371408.1:n.1097+59G=