Canonical Allele Identifier: CA1146921891
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704253_230704257delinsGGCGG , CM000663.2:g.230704253_230704257delinsGGCGG GRCh38
NC_000001.10:g.230839999_230840003delinsGGCGG , CM000663.1:g.230839999_230840003delinsGGCGG GRCh37
NC_000001.9:g.228906622_228906626delinsGGCGG NCBI36
NG_008836.1:g.15334_15338delinsCCGCC
NG_008836.2:g.15334_15338delinsCCGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1178_1182delinsCCGCC MANE Select ENSP00000355627.5:p.Pro393=
ENST00000679684.1:c.1178_1182delinsCCGCC ENSP00000505981.1:p.Pro393=
ENST00000679738.1:c.1178_1182delinsCCGCC ENSP00000505063.1:p.Pro393=
ENST00000679802.1:c.*637_*641delinsCCGCC ENSP00000505184.1:n.*637_*641delinsCCGCC
ENST00000679854.1:n.5483_5487delinsCCGCC
ENST00000679957.1:c.1178_1182delinsCCGCC ENSP00000506646.1:p.Pro393=
ENST00000680041.1:c.1178_1182delinsCCGCC ENSP00000504866.1:p.Pro393=
ENST00000680783.1:c.829+5738_829+5742delinsCCGCC ENSP00000506329.1:n.829+5738_829+5742deli...
ENST00000681269.1:c.1178_1182delinsCCGCC ENSP00000505985.1:p.Pro393=
ENST00000681347.1:n.3284_3288delinsCCGCC
ENST00000681514.1:c.1178_1182delinsCCGCC ENSP00000505963.1:p.Pro393=
ENST00000681772.1:c.*672_*676delinsCCGCC ENSP00000505829.1:n.*672_*676delinsCCGCC
ENST00000366667.4:c.1205_1209delinsCCGCC ENSP00000355627.4:p.Pro402=
NM_000029.3:c.1205_1209delinsCCGCC NP_000020.1:p.Pro402=
NM_000029.4:c.1205_1209delinsCCGCC NP_000020.1:p.Pro402=
NM_001382817.3:c.1178_1182delinsCCGCC NP_001369746.2:p.Pro393=
NM_001384479.1:c.1178_1182delinsCCGCC MANE Select NP_001371408.1:p.Pro393=