Canonical Allele Identifier: CA1226668864
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230708380_230708383delinsTCTC , CM000663.2:g.230708380_230708383delinsTCTC GRCh38
NC_000001.10:g.230844126_230844129delinsTCTC , CM000663.1:g.230844126_230844129delinsTCTC GRCh37
NC_000001.9:g.228910749_228910752delinsTCTC NCBI36
NG_008836.1:g.11208_11211delinsGAGA
NG_008836.2:g.11208_11211delinsGAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.829+1612_829+1615delinsGAGA MANE Select ENSP00000355627.5:n.829+1612_829+1615deli...
ENST00000679684.1:c.829+1612_829+1615delinsGAGA ENSP00000505981.1:n.829+1612_829+1615deli...
ENST00000679738.1:c.829+1612_829+1615delinsGAGA ENSP00000505063.1:n.829+1612_829+1615deli...
ENST00000679802.1:c.*288+724_*288+727delinsGAGA ENSP00000505184.1:n.*288+724_*288+727deli...
ENST00000679854.1:n.2952_2955delinsGAGA
ENST00000679957.1:c.829+1612_829+1615delinsGAGA ENSP00000506646.1:n.829+1612_829+1615deli...
ENST00000680041.1:c.829+1612_829+1615delinsGAGA ENSP00000504866.1:n.829+1612_829+1615deli...
ENST00000680783.1:c.829+1612_829+1615delinsGAGA ENSP00000506329.1:n.829+1612_829+1615deli...
ENST00000681269.1:c.829+1612_829+1615delinsGAGA ENSP00000505985.1:n.829+1612_829+1615deli...
ENST00000681347.1:n.1340+1612_1340+1615delinsGAGA
ENST00000681514.1:c.829+1612_829+1615delinsGAGA ENSP00000505963.1:n.829+1612_829+1615deli...
ENST00000681772.1:c.829+1612_829+1615delinsGAGA ENSP00000505829.1:n.829+1612_829+1615deli...
ENST00000366667.4:c.856+1612_856+1615delinsGAGA ENSP00000355627.4:n.856+1612_856+1615deli...
NM_000029.3:c.856+1612_856+1615delinsGAGA NP_000020.1:n.856+1612_856+1615delinsGAGA...
NM_000029.4:c.856+1612_856+1615delinsGAGA NP_000020.1:n.856+1612_856+1615delinsGAGA...
NM_001382817.3:c.829+1612_829+1615delinsGAGA NP_001369746.2:n.829+1612_829+1615delinsG...
NM_001384479.1:c.829+1612_829+1615delinsGAGA MANE Select NP_001371408.1:n.829+1612_829+1615delinsG...