Canonical Allele Identifier: CA2650970586

Gene: AGT

Linked Data

• gnomAD v4: 1-230702642-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702642T>A , CM000663.2:g.230702642T>A	GRCh38
NC_000001.10:g.230838388T>A , CM000663.1:g.230838388T>A	GRCh37
NC_000001.9:g.228905011T>A	NCBI36
NG_008836.1:g.16949A>T
NG_008836.2:g.16949A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*499A>T MANE Select	ENSP00000355627.5:n.*499A>T
ENST00000679738.1:c.*499A>T	ENSP00000505063.1:n.*499A>T
ENST00000679802.1:c.*1389A>T	ENSP00000505184.1:n.*1389A>T
ENST00000679854.1:n.6235A>T
ENST00000680041.1:c.*499A>T	ENSP00000504866.1:n.*499A>T
ENST00000680783.1:c.829+7353A>T	ENSP00000506329.1:n.829+7353A>T
ENST00000681269.1:c.*499A>T	ENSP00000505985.1:n.*499A>T
ENST00000681347.1:n.4036A>T
ENST00000681514.1:c.*499A>T	ENSP00000505963.1:n.*499A>T
ENST00000681772.1:c.*1424A>T	ENSP00000505829.1:n.*1424A>T
ENST00000366667.4:c.*499A>T	ENSP00000355627.4:n.*499A>T
NM_000029.3:c.*499A>T	NP_000020.1:n.*499A>T
NM_000029.4:c.*499A>T	NP_000020.1:n.*499A>T
NM_001382817.3:c.*499A>T	NP_001369746.2:n.*499A>T
NM_001384479.1:c.*499A>T MANE Select	NP_001371408.1:n.*499A>T