Canonical Allele Identifier: CA423883530

Gene: AGT

Linked Data

• gnomAD v4: 1-230704277-C-A
• MyVariant Identifiers: chr1:g.230840023C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704277C>A , CM000663.2:g.230704277C>A	GRCh38
NC_000001.10:g.230840023C>A , CM000663.1:g.230840023C>A	GRCh37
NC_000001.9:g.228906646C>A	NCBI36
NG_008836.1:g.15314G>T
NG_008836.2:g.15314G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1158G>T MANE Select	ENSP00000355627.5:p.Leu386=
ENST00000679684.1:c.1158G>T	ENSP00000505981.1:p.Leu386=
ENST00000679738.1:c.1158G>T	ENSP00000505063.1:p.Leu386=
ENST00000679802.1:c.*617G>T	ENSP00000505184.1:n.*617G>T
ENST00000679854.1:n.5463G>T
ENST00000679957.1:c.1158G>T	ENSP00000506646.1:p.Leu386=
ENST00000680041.1:c.1158G>T	ENSP00000504866.1:p.Leu386=
ENST00000680783.1:c.829+5718G>T	ENSP00000506329.1:n.829+5718G>T
ENST00000681269.1:c.1158G>T	ENSP00000505985.1:p.Leu386=
ENST00000681347.1:n.3264G>T
ENST00000681514.1:c.1158G>T	ENSP00000505963.1:p.Leu386=
ENST00000681772.1:c.*652G>T	ENSP00000505829.1:n.*652G>T
ENST00000366667.4:c.1185G>T	ENSP00000355627.4:p.Leu395=
NM_000029.3:c.1185G>T	NP_000020.1:p.Leu395=
NM_000029.4:c.1185G>T	NP_000020.1:p.Leu395=
NM_001382817.3:c.1158G>T	NP_001369746.2:p.Leu386=
NM_001384479.1:c.1158G>T MANE Select	NP_001371408.1:p.Leu386=