Canonical Allele Identifier: CA2650970458

Gene: AGT

Linked Data

• gnomAD v4: 1-230702550-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702550T>G , CM000663.2:g.230702550T>G	GRCh38
NC_000001.10:g.230838296T>G , CM000663.1:g.230838296T>G	GRCh37
NC_000001.9:g.228904919T>G	NCBI36
NG_008836.1:g.17041A>C
NG_008836.2:g.17041A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*591A>C MANE Select	ENSP00000355627.5:n.*591A>C
ENST00000679738.1:c.*591A>C	ENSP00000505063.1:n.*591A>C
ENST00000679802.1:c.*1481A>C	ENSP00000505184.1:n.*1481A>C
ENST00000679854.1:n.6327A>C
ENST00000680041.1:c.*591A>C	ENSP00000504866.1:n.*591A>C
ENST00000680783.1:c.829+7445A>C	ENSP00000506329.1:n.829+7445A>C
ENST00000681269.1:c.*591A>C	ENSP00000505985.1:n.*591A>C
ENST00000681347.1:n.4128A>C
ENST00000681514.1:c.*591A>C	ENSP00000505963.1:n.*591A>C
ENST00000681772.1:c.*1516A>C	ENSP00000505829.1:n.*1516A>C
ENST00000366667.4:c.*591A>C	ENSP00000355627.4:n.*591A>C
NM_000029.3:c.*591A>C	NP_000020.1:n.*591A>C
NM_000029.4:c.*591A>C	NP_000020.1:n.*591A>C
NM_001382817.3:c.*591A>C	NP_001369746.2:n.*591A>C
NM_001384479.1:c.*591A>C MANE Select	NP_001371408.1:n.*591A>C