Canonical Allele Identifier: CA2650970691
Gene: AGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704191dup , CM000663.2:g.230704191dup GRCh38
NC_000001.10:g.230839937dup , CM000663.1:g.230839937dup GRCh37
NC_000001.9:g.228906560dup NCBI36
NG_008836.1:g.15400dup
NG_008836.2:g.15400dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.1242+2dup MANE Select ENSP00000355627.5:n.1242+2dup
ENST00000679684.1:c.1242+2dup ENSP00000505981.1:n.1242+2dup
ENST00000679738.1:c.1242+2dup ENSP00000505063.1:n.1242+2dup
ENST00000679802.1:c.*701+2dup ENSP00000505184.1:n.*701+2dup
ENST00000679854.1:n.5547+2dup
ENST00000679957.1:c.1233+11dup ENSP00000506646.1:n.1233+11dup
ENST00000680041.1:c.1242+2dup ENSP00000504866.1:n.1242+2dup
ENST00000680783.1:c.829+5804dup ENSP00000506329.1:n.829+5804dup
ENST00000681269.1:c.1242+2dup ENSP00000505985.1:n.1242+2dup
ENST00000681347.1:n.3348+2dup
ENST00000681514.1:c.1242+2dup ENSP00000505963.1:n.1242+2dup
ENST00000681772.1:c.*736+2dup ENSP00000505829.1:n.*736+2dup
ENST00000366667.4:c.1269+2dup ENSP00000355627.4:n.1269+2dup
NM_000029.3:c.1269+2dup NP_000020.1:n.1269+2dup
NM_000029.4:c.1269+2dup NP_000020.1:n.1269+2dup
NM_001382817.3:c.1242+2dup NP_001369746.2:n.1242+2dup
NM_001384479.1:c.1242+2dup MANE Select NP_001371408.1:n.1242+2dup