Canonical Allele Identifier: CA1409909230

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741091C= , CM000665.2:g.148741091C=	GRCh38
NC_000003.11:g.148458878C= , CM000665.1:g.148458878C=	GRCh37
NC_000003.10:g.149941568C=	NCBI36
NG_008468.1:g.48221C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.56C= MANE Select	ENSP00000273430.3:p.Pro19=
ENST00000402260.2:c.56C=	ENSP00000385641.3:p.Pro19=
ENST00000418473.7:c.56C=	ENSP00000398832.4:p.Pro19=
ENST00000349243.7:c.56C=	ENSP00000273430.3:p.Pro19=
ENST00000402260.1:c.143C=	ENSP00000385641.2:p.Pro48=
ENST00000404754.2:c.56C=	ENSP00000385612.2:p.Pro19=
ENST00000418473.6:c.161C=	ENSP00000398832.3:p.Pro54=
ENST00000461609.1:c.56C=	ENSP00000418851.1:p.Pro19=
ENST00000474935.5:c.56C=	ENSP00000418084.1:p.Pro19=
ENST00000475347.5:c.56C=	ENSP00000419783.1:p.Pro19=
ENST00000497524.5:c.56C=	ENSP00000419422.1:p.Pro19=
NM_000685.4:c.56C=	NP_000676.1:p.Pro19=
NM_004835.4:c.161C=	NP_004826.5:p.Pro54=
NM_009585.3:c.56C=	NP_033611.1:p.Pro19=
NM_031850.3:c.161C=	NP_114038.4:p.Pro54=
NM_032049.3:c.143C=	NP_114438.2:p.Pro48=
NM_000685.5:c.56C= MANE Select	NP_000676.1:p.Pro19=
NM_001382736.1:c.56C=	NP_001369665.1:p.Pro19=
NM_001382737.1:c.56C=	NP_001369666.1:p.Pro19=
NM_004835.5:c.56C=	NP_004826.6:p.Pro19=
NM_009585.4:c.56C=	NP_033611.1:p.Pro19=
NM_031850.4:c.56C=	NP_114038.5:p.Pro19=
NM_032049.4:c.56C=	NP_114438.3:p.Pro19=