Canonical Allele Identifier: CA2695196781

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704258_230704280dup , CM000663.2:g.230704258_230704280dup	GRCh38
NC_000001.10:g.230840004_230840026dup , CM000663.1:g.230840004_230840026dup	GRCh37
NC_000001.9:g.228906627_228906649dup	NCBI36
NG_008836.1:g.15313_15335dup
NG_008836.2:g.15313_15335dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1157_1179dup MANE Select	ENSP00000355627.5:p.Ala394CysfsTer15
ENST00000679684.1:c.1157_1179dup	ENSP00000505981.1:p.Ala394CysfsTer15
ENST00000679738.1:c.1157_1179dup	ENSP00000505063.1:p.Ala394CysfsTer15
ENST00000679802.1:c.*616_*638dup	ENSP00000505184.1:n.*616_*638dup
ENST00000679854.1:n.5462_5484dup
ENST00000679957.1:c.1157_1179dup	ENSP00000506646.1:p.Ala394CysfsTer15
ENST00000680041.1:c.1157_1179dup	ENSP00000504866.1:p.Ala394CysfsTer15
ENST00000680783.1:c.829+5717_829+5739dup	ENSP00000506329.1:n.829+5717_829+5739dup
ENST00000681269.1:c.1157_1179dup	ENSP00000505985.1:p.Ala394CysfsTer15
ENST00000681347.1:n.3263_3285dup
ENST00000681514.1:c.1157_1179dup	ENSP00000505963.1:p.Ala394CysfsTer15
ENST00000681772.1:c.*651_*673dup	ENSP00000505829.1:n.*651_*673dup
ENST00000366667.4:c.1184_1206dup	ENSP00000355627.4:p.Ala403CysfsTer15
NM_000029.3:c.1184_1206dup	NP_000020.1:p.Ala403CysfsTer15
NM_000029.4:c.1184_1206dup	NP_000020.1:p.Ala403CysfsTer15
NM_001382817.3:c.1157_1179dup	NP_001369746.2:p.Ala394CysfsTer15
NM_001384479.1:c.1157_1179dup MANE Select	NP_001371408.1:p.Ala394CysfsTer15