Canonical Allele Identifier: CA1140726481

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704219T= , CM000663.2:g.230704219T=	GRCh38
NC_000001.10:g.230839965T= , CM000663.1:g.230839965T=	GRCh37
NC_000001.9:g.228906588T=	NCBI36
NG_008836.1:g.15372A=
NG_008836.2:g.15372A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1216A= MANE Select	ENSP00000355627.5:p.Ser406=
ENST00000679684.1:c.1216A=	ENSP00000505981.1:p.Ser406=
ENST00000679738.1:c.1216A=	ENSP00000505063.1:p.Ser406=
ENST00000679802.1:c.*675A=	ENSP00000505184.1:n.*675A=
ENST00000679854.1:n.5521A=
ENST00000679957.1:c.1216A=	ENSP00000506646.1:p.Ser406=
ENST00000680041.1:c.1216A=	ENSP00000504866.1:p.Ser406=
ENST00000680783.1:c.829+5776A=	ENSP00000506329.1:n.829+5776A=
ENST00000681269.1:c.1216A=	ENSP00000505985.1:p.Ser406=
ENST00000681347.1:n.3322A=
ENST00000681514.1:c.1216A=	ENSP00000505963.1:p.Ser406=
ENST00000681772.1:c.*710A=	ENSP00000505829.1:n.*710A=
ENST00000366667.4:c.1243A=	ENSP00000355627.4:p.Ser415=
NM_000029.3:c.1243A=	NP_000020.1:p.Ser415=
NM_000029.4:c.1243A=	NP_000020.1:p.Ser415=
NM_001382817.3:c.1216A=	NP_001369746.2:p.Ser406=
NM_001384479.1:c.1216A= MANE Select	NP_001371408.1:p.Ser406=