Canonical Allele Identifier: CA345201926

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230838912A>G (hg19) ; chr1:g.230703166A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703166A>G , CM000663.2:g.230703166A>G	GRCh38
NC_000001.10:g.230838912A>G , CM000663.1:g.230838912A>G	GRCh37
NC_000001.9:g.228905535A>G	NCBI36
NG_008836.1:g.16425T>C
NG_008836.2:g.16425T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1406T>C MANE Select	ENSP00000355627.5:p.Val469Ala
ENST00000679738.1:c.1406T>C	ENSP00000505063.1:p.Val469Ala
ENST00000679802.1:c.*865T>C	ENSP00000505184.1:n.*865T>C
ENST00000679854.1:n.5711T>C
ENST00000679957.1:c.1397T>C	ENSP00000506646.1:p.Val466Ala
ENST00000680041.1:c.1406T>C	ENSP00000504866.1:p.Val469Ala
ENST00000680783.1:c.829+6829T>C	ENSP00000506329.1:n.829+6829T>C
ENST00000681269.1:c.1406T>C	ENSP00000505985.1:p.Val469Ala
ENST00000681347.1:n.3512T>C
ENST00000681514.1:c.1406T>C	ENSP00000505963.1:p.Val469Ala
ENST00000681772.1:c.*900T>C	ENSP00000505829.1:n.*900T>C
ENST00000366667.4:c.1433T>C	ENSP00000355627.4:p.Val478Ala
NM_000029.3:c.1433T>C	NP_000020.1:p.Val478Ala
NM_000029.4:c.1433T>C	NP_000020.1:p.Val478Ala
NM_001382817.3:c.1406T>C	NP_001369746.2:p.Val469Ala
NM_001384479.1:c.1406T>C MANE Select	NP_001371408.1:p.Val469Ala