Canonical Allele Identifier: CA345203347

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230840052G>C (hg19) ; chr1:g.230704306G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704306G>C , CM000663.2:g.230704306G>C	GRCh38
NC_000001.10:g.230840052G>C , CM000663.1:g.230840052G>C	GRCh37
NC_000001.9:g.228906675G>C	NCBI36
NG_008836.1:g.15285C>G
NG_008836.2:g.15285C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1129C>G MANE Select	ENSP00000355627.5:p.Leu377Val
ENST00000679684.1:c.1129C>G	ENSP00000505981.1:p.Leu377Val
ENST00000679738.1:c.1129C>G	ENSP00000505063.1:p.Leu377Val
ENST00000679802.1:c.*588C>G	ENSP00000505184.1:n.*588C>G
ENST00000679854.1:n.5434C>G
ENST00000679957.1:c.1129C>G	ENSP00000506646.1:p.Leu377Val
ENST00000680041.1:c.1129C>G	ENSP00000504866.1:p.Leu377Val
ENST00000680783.1:c.829+5689C>G	ENSP00000506329.1:n.829+5689C>G
ENST00000681269.1:c.1129C>G	ENSP00000505985.1:p.Leu377Val
ENST00000681347.1:n.3235C>G
ENST00000681514.1:c.1129C>G	ENSP00000505963.1:p.Leu377Val
ENST00000681772.1:c.*623C>G	ENSP00000505829.1:n.*623C>G
ENST00000366667.4:c.1156C>G	ENSP00000355627.4:p.Leu386Val
NM_000029.3:c.1156C>G	NP_000020.1:p.Leu386Val
NM_000029.4:c.1156C>G	NP_000020.1:p.Leu386Val
NM_001382817.3:c.1129C>G	NP_001369746.2:p.Leu377Val
NM_001384479.1:c.1129C>G MANE Select	NP_001371408.1:p.Leu377Val