Canonical Allele Identifier: CA1013238290
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663369494

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705876dup , CM000663.2:g.230705876dup GRCh38
NC_000001.10:g.230841622dup , CM000663.1:g.230841622dup GRCh37
NC_000001.9:g.228908245dup NCBI36
NG_008836.1:g.13719dup
NG_008836.2:g.13719dup

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1097+61dup MANE Select ENSP00000355627.5:n.1097+61dup
ENST00000679684.1:c.1097+61dup ENSP00000505981.1:n.1097+61dup
ENST00000679738.1:c.1097+61dup ENSP00000505063.1:n.1097+61dup
ENST00000679802.1:c.*556+61dup ENSP00000505184.1:n.*556+61dup
ENST00000679854.1:n.5402+61dup
ENST00000679957.1:c.1097+61dup ENSP00000506646.1:n.1097+61dup
ENST00000680041.1:c.1097+61dup ENSP00000504866.1:n.1097+61dup
ENST00000680783.1:c.829+4123dup ENSP00000506329.1:n.829+4123dup
ENST00000681269.1:c.1097+61dup ENSP00000505985.1:n.1097+61dup
ENST00000681347.1:n.1669dup
ENST00000681514.1:c.1097+61dup ENSP00000505963.1:n.1097+61dup
ENST00000681772.1:c.*57dup ENSP00000505829.1:n.*57dup
ENST00000366667.4:c.1124+61dup ENSP00000355627.4:n.1124+61dup
NM_000029.3:c.1124+61dup NP_000020.1:n.1124+61dup
NM_000029.4:c.1124+61dup NP_000020.1:n.1124+61dup
NM_001382817.3:c.1097+61dup NP_001369746.2:n.1097+61dup
NM_001384479.1:c.1097+61dup MANE Select NP_001371408.1:n.1097+61dup