Canonical Allele Identifier: CA423883519
Gene: AGT HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.230840005C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704259C>T , CM000663.2:g.230704259C>T GRCh38
NC_000001.10:g.230840005C>T , CM000663.1:g.230840005C>T GRCh37
NC_000001.9:g.228906628C>T NCBI36
NG_008836.1:g.15332G>A
NG_008836.2:g.15332G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1176G>A MANE Select ENSP00000355627.5:p.Leu392=
ENST00000679684.1:c.1176G>A ENSP00000505981.1:p.Leu392=
ENST00000679738.1:c.1176G>A ENSP00000505063.1:p.Leu392=
ENST00000679802.1:c.*635G>A ENSP00000505184.1:n.*635G>A
ENST00000679854.1:n.5481G>A
ENST00000679957.1:c.1176G>A ENSP00000506646.1:p.Leu392=
ENST00000680041.1:c.1176G>A ENSP00000504866.1:p.Leu392=
ENST00000680783.1:c.829+5736G>A ENSP00000506329.1:n.829+5736G>A
ENST00000681269.1:c.1176G>A ENSP00000505985.1:p.Leu392=
ENST00000681347.1:n.3282G>A
ENST00000681514.1:c.1176G>A ENSP00000505963.1:p.Leu392=
ENST00000681772.1:c.*670G>A ENSP00000505829.1:n.*670G>A
ENST00000366667.4:c.1203G>A ENSP00000355627.4:p.Leu401=
NM_000029.3:c.1203G>A NP_000020.1:p.Leu401=
NM_000029.4:c.1203G>A NP_000020.1:p.Leu401=
NM_001382817.3:c.1176G>A NP_001369746.2:p.Leu392=
NM_001384479.1:c.1176G>A MANE Select NP_001371408.1:p.Leu392=