Canonical Allele Identifier: CA891862742

Gene: AGT

Linked Data

• ClinVar Variation Id: 591565
• ClinVar RCV Id: RCV000722746
• dbSNP Id: rs1558288004

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710340_230710353dup , CM000663.2:g.230710340_230710353dup	GRCh38
NC_000001.10:g.230846086_230846099dup , CM000663.1:g.230846086_230846099dup	GRCh37
NC_000001.9:g.228912709_228912722dup	NCBI36
NG_008836.1:g.9239_9252dup
NG_008836.2:g.9239_9252dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.472_485dup MANE Select	ENSP00000355627.5:p.Cys162Ter
ENST00000679684.1:c.472_485dup	ENSP00000505981.1:p.Cys162Ter
ENST00000679738.1:c.472_485dup	ENSP00000505063.1:p.Cys162Ter
ENST00000679802.1:c.472_485dup	ENSP00000505184.1:p.Cys162Ter
ENST00000679854.1:n.983_996dup
ENST00000679957.1:c.472_485dup	ENSP00000506646.1:p.Cys162Ter
ENST00000680041.1:c.472_485dup	ENSP00000504866.1:p.Cys162Ter
ENST00000680783.1:c.472_485dup	ENSP00000506329.1:p.Cys162Ter
ENST00000681269.1:c.472_485dup	ENSP00000505985.1:p.Cys162Ter
ENST00000681347.1:n.983_996dup
ENST00000681514.1:c.472_485dup	ENSP00000505963.1:p.Cys162Ter
ENST00000681772.1:c.472_485dup	ENSP00000505829.1:p.Cys162Ter
ENST00000366667.4:c.499_512dup	ENSP00000355627.4:p.Cys171Ter
NM_000029.3:c.499_512dup	NP_000020.1:p.Cys171Ter
NM_000029.4:c.499_512dup	NP_000020.1:p.Cys171Ter
NM_001382817.3:c.472_485dup	NP_001369746.2:p.Cys162Ter
NM_001384479.1:c.472_485dup MANE Select	NP_001371408.1:p.Cys162Ter