Canonical Allele Identifier: CA345202313

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230838993A>T (hg19) ; chr1:g.230703247A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703247A>T , CM000663.2:g.230703247A>T	GRCh38
NC_000001.10:g.230838993A>T , CM000663.1:g.230838993A>T	GRCh37
NC_000001.9:g.228905616A>T	NCBI36
NG_008836.1:g.16344T>A
NG_008836.2:g.16344T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1325T>A MANE Select	ENSP00000355627.5:p.Val442Asp
ENST00000679738.1:c.1325T>A	ENSP00000505063.1:p.Val442Asp
ENST00000679802.1:c.*784T>A	ENSP00000505184.1:n.*784T>A
ENST00000679854.1:n.5630T>A
ENST00000679957.1:c.1316T>A	ENSP00000506646.1:p.Val439Asp
ENST00000680041.1:c.1325T>A	ENSP00000504866.1:p.Val442Asp
ENST00000680783.1:c.829+6748T>A	ENSP00000506329.1:n.829+6748T>A
ENST00000681269.1:c.1325T>A	ENSP00000505985.1:p.Val442Asp
ENST00000681347.1:n.3431T>A
ENST00000681514.1:c.1325T>A	ENSP00000505963.1:p.Val442Asp
ENST00000681772.1:c.*819T>A	ENSP00000505829.1:n.*819T>A
ENST00000366667.4:c.1352T>A	ENSP00000355627.4:p.Val451Asp
NM_000029.3:c.1352T>A	NP_000020.1:p.Val451Asp
NM_000029.4:c.1352T>A	NP_000020.1:p.Val451Asp
NM_001382817.3:c.1325T>A	NP_001369746.2:p.Val442Asp
NM_001384479.1:c.1325T>A MANE Select	NP_001371408.1:p.Val442Asp