Canonical Allele Identifier: CA345202187

Gene: AGT

Linked Data

• ClinVar Variation Id: 2690863
• ClinVar RCV Id: RCV003489541
• MyVariant Identifiers: chr1:g.230838967A>T (hg19) ; chr1:g.230703221A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703221A>T , CM000663.2:g.230703221A>T	GRCh38
NC_000001.10:g.230838967A>T , CM000663.1:g.230838967A>T	GRCh37
NC_000001.9:g.228905590A>T	NCBI36
NG_008836.1:g.16370T>A
NG_008836.2:g.16370T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1351T>A MANE Select	ENSP00000355627.5:p.Phe451Ile
ENST00000679738.1:c.1351T>A	ENSP00000505063.1:p.Phe451Ile
ENST00000679802.1:c.*810T>A	ENSP00000505184.1:n.*810T>A
ENST00000679854.1:n.5656T>A
ENST00000679957.1:c.1342T>A	ENSP00000506646.1:p.Phe448Ile
ENST00000680041.1:c.1351T>A	ENSP00000504866.1:p.Phe451Ile
ENST00000680783.1:c.829+6774T>A	ENSP00000506329.1:n.829+6774T>A
ENST00000681269.1:c.1351T>A	ENSP00000505985.1:p.Phe451Ile
ENST00000681347.1:n.3457T>A
ENST00000681514.1:c.1351T>A	ENSP00000505963.1:p.Phe451Ile
ENST00000681772.1:c.*845T>A	ENSP00000505829.1:n.*845T>A
ENST00000366667.4:c.1378T>A	ENSP00000355627.4:p.Phe460Ile
NM_000029.3:c.1378T>A	NP_000020.1:p.Phe460Ile
NM_000029.4:c.1378T>A	NP_000020.1:p.Phe460Ile
NM_001382817.3:c.1351T>A	NP_001369746.2:p.Phe451Ile
NM_001384479.1:c.1351T>A MANE Select	NP_001371408.1:p.Phe451Ile