Canonical Allele Identifier: CA423883548

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230840047T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704301T>C , CM000663.2:g.230704301T>C	GRCh38
NC_000001.10:g.230840047T>C , CM000663.1:g.230840047T>C	GRCh37
NC_000001.9:g.228906670T>C	NCBI36
NG_008836.1:g.15290A>G
NG_008836.2:g.15290A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1134A>G MANE Select	ENSP00000355627.5:p.Gln378=
ENST00000679684.1:c.1134A>G	ENSP00000505981.1:p.Gln378=
ENST00000679738.1:c.1134A>G	ENSP00000505063.1:p.Gln378=
ENST00000679802.1:c.*593A>G	ENSP00000505184.1:n.*593A>G
ENST00000679854.1:n.5439A>G
ENST00000679957.1:c.1134A>G	ENSP00000506646.1:p.Gln378=
ENST00000680041.1:c.1134A>G	ENSP00000504866.1:p.Gln378=
ENST00000680783.1:c.829+5694A>G	ENSP00000506329.1:n.829+5694A>G
ENST00000681269.1:c.1134A>G	ENSP00000505985.1:p.Gln378=
ENST00000681347.1:n.3240A>G
ENST00000681514.1:c.1134A>G	ENSP00000505963.1:p.Gln378=
ENST00000681772.1:c.*628A>G	ENSP00000505829.1:n.*628A>G
ENST00000366667.4:c.1161A>G	ENSP00000355627.4:p.Gln387=
NM_000029.3:c.1161A>G	NP_000020.1:p.Gln387=
NM_000029.4:c.1161A>G	NP_000020.1:p.Gln387=
NM_001382817.3:c.1134A>G	NP_001369746.2:p.Gln378=
NM_001384479.1:c.1134A>G MANE Select	NP_001371408.1:p.Gln378=