Canonical Allele Identifier: CA1409910755

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742387A= , CM000665.2:g.148742387A=	GRCh38
NC_000003.11:g.148460174A= , CM000665.1:g.148460174A=	GRCh37
NC_000003.10:g.149942864A=	NCBI36
NG_008468.1:g.49517A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*272A= MANE Select	ENSP00000273430.3:n.*272A=
ENST00000402260.2:c.*272A=	ENSP00000385641.3:n.*272A=
ENST00000418473.7:c.*272A=	ENSP00000398832.4:n.*272A=
ENST00000349243.7:c.*272A=	ENSP00000273430.3:n.*272A=
ENST00000402260.1:c.*272A=	ENSP00000385641.2:n.*272A=
ENST00000404754.2:c.*272A=	ENSP00000385612.2:n.*272A=
ENST00000418473.6:c.1457A=	ENSP00000398832.3:n.1457A=
ENST00000497524.5:c.*272A=	ENSP00000419422.1:n.*272A=
NM_000685.4:c.*272A=	NP_000676.1:n.*272A=
NM_004835.4:c.*272A=	NP_004826.5:n.*272A=
NM_009585.3:c.*272A=	NP_033611.1:n.*272A=
NM_031850.3:c.*272A=	NP_114038.4:n.*272A=
NM_032049.3:c.*272A=	NP_114438.2:n.*272A=
NM_000685.5:c.*272A= MANE Select	NP_000676.1:n.*272A=
NM_001382736.1:c.*272A=	NP_001369665.1:n.*272A=
NM_001382737.1:c.*272A=	NP_001369666.1:n.*272A=
NM_004835.5:c.*272A=	NP_004826.6:n.*272A=
NM_009585.4:c.*272A=	NP_033611.1:n.*272A=
NM_031850.4:c.*272A=	NP_114038.5:n.*272A=
NM_032049.4:c.*272A=	NP_114438.3:n.*272A=