Canonical Allele Identifier: CA345203259

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230840015T>C (hg19) ; chr1:g.230704269T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704269T>C , CM000663.2:g.230704269T>C	GRCh38
NC_000001.10:g.230840015T>C , CM000663.1:g.230840015T>C	GRCh37
NC_000001.9:g.228906638T>C	NCBI36
NG_008836.1:g.15322A>G
NG_008836.2:g.15322A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1166A>G MANE Select	ENSP00000355627.5:p.Gln389Arg
ENST00000679684.1:c.1166A>G	ENSP00000505981.1:p.Gln389Arg
ENST00000679738.1:c.1166A>G	ENSP00000505063.1:p.Gln389Arg
ENST00000679802.1:c.*625A>G	ENSP00000505184.1:n.*625A>G
ENST00000679854.1:n.5471A>G
ENST00000679957.1:c.1166A>G	ENSP00000506646.1:p.Gln389Arg
ENST00000680041.1:c.1166A>G	ENSP00000504866.1:p.Gln389Arg
ENST00000680783.1:c.829+5726A>G	ENSP00000506329.1:n.829+5726A>G
ENST00000681269.1:c.1166A>G	ENSP00000505985.1:p.Gln389Arg
ENST00000681347.1:n.3272A>G
ENST00000681514.1:c.1166A>G	ENSP00000505963.1:p.Gln389Arg
ENST00000681772.1:c.*660A>G	ENSP00000505829.1:n.*660A>G
ENST00000366667.4:c.1193A>G	ENSP00000355627.4:p.Gln398Arg
NM_000029.3:c.1193A>G	NP_000020.1:p.Gln398Arg
NM_000029.4:c.1193A>G	NP_000020.1:p.Gln398Arg
NM_001382817.3:c.1166A>G	NP_001369746.2:p.Gln389Arg
NM_001384479.1:c.1166A>G MANE Select	NP_001371408.1:p.Gln389Arg