Canonical Allele Identifier: CA345201995

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230838934C>A (hg19) ; chr1:g.230703188C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703188C>A , CM000663.2:g.230703188C>A	GRCh38
NC_000001.10:g.230838934C>A , CM000663.1:g.230838934C>A	GRCh37
NC_000001.9:g.228905557C>A	NCBI36
NG_008836.1:g.16403G>T
NG_008836.2:g.16403G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1384G>T MANE Select	ENSP00000355627.5:p.Ala462Ser
ENST00000679738.1:c.1384G>T	ENSP00000505063.1:p.Ala462Ser
ENST00000679802.1:c.*843G>T	ENSP00000505184.1:n.*843G>T
ENST00000679854.1:n.5689G>T
ENST00000679957.1:c.1375G>T	ENSP00000506646.1:p.Ala459Ser
ENST00000680041.1:c.1384G>T	ENSP00000504866.1:p.Ala462Ser
ENST00000680783.1:c.829+6807G>T	ENSP00000506329.1:n.829+6807G>T
ENST00000681269.1:c.1384G>T	ENSP00000505985.1:p.Ala462Ser
ENST00000681347.1:n.3490G>T
ENST00000681514.1:c.1384G>T	ENSP00000505963.1:p.Ala462Ser
ENST00000681772.1:c.*878G>T	ENSP00000505829.1:n.*878G>T
ENST00000366667.4:c.1411G>T	ENSP00000355627.4:p.Ala471Ser
NM_000029.3:c.1411G>T	NP_000020.1:p.Ala471Ser
NM_000029.4:c.1411G>T	NP_000020.1:p.Ala471Ser
NM_001382817.3:c.1384G>T	NP_001369746.2:p.Ala462Ser
NM_001384479.1:c.1384G>T MANE Select	NP_001371408.1:p.Ala462Ser