Canonical Allele Identifier: CA1226667857

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230706195T= , CM000663.2:g.230706195T=	GRCh38
NC_000001.10:g.230841941T= , CM000663.1:g.230841941T=	GRCh37
NC_000001.9:g.228908564T=	NCBI36
NG_008836.1:g.13396A=
NG_008836.2:g.13396A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.835A= MANE Select	ENSP00000355627.5:p.Met279=
ENST00000679684.1:c.835A=	ENSP00000505981.1:p.Met279=
ENST00000679738.1:c.835A=	ENSP00000505063.1:p.Met279=
ENST00000679802.1:c.*294A=	ENSP00000505184.1:n.*294A=
ENST00000679854.1:n.5140A=
ENST00000679957.1:c.835A=	ENSP00000506646.1:p.Met279=
ENST00000680041.1:c.835A=	ENSP00000504866.1:p.Met279=
ENST00000680783.1:c.829+3800A=	ENSP00000506329.1:n.829+3800A=
ENST00000681269.1:c.835A=	ENSP00000505985.1:p.Met279=
ENST00000681347.1:n.1346A=
ENST00000681514.1:c.835A=	ENSP00000505963.1:p.Met279=
ENST00000681772.1:c.835A=	ENSP00000505829.1:p.Met279=
ENST00000366667.4:c.862A=	ENSP00000355627.4:p.Met288=
NM_000029.3:c.862A=	NP_000020.1:p.Met288=
NM_000029.4:c.862A=	NP_000020.1:p.Met288=
NM_001382817.3:c.835A=	NP_001369746.2:p.Met279=
NM_001384479.1:c.835A= MANE Select	NP_001371408.1:p.Met279=