Canonical Allele Identifier: CA10617597
Gene: AGTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148698075C>A , CM000665.2:g.148698075C>A GRCh38
NC_000003.11:g.148415862C>A , CM000665.1:g.148415862C>A GRCh37
NC_000003.10:g.149898552C>A NCBI36
NG_008468.1:g.5205C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.-184C>A MANE Select ENSP00000273430.3:n.-184C>A
ENST00000418473.7:c.-158C>A ENSP00000398832.4:n.-158C>A
ENST00000349243.7:c.-184C>A ENSP00000273430.3:n.-184C>A
ENST00000404754.2:c.-122C>A ENSP00000385612.2:n.-122C>A
ENST00000497524.5:c.-100C>A ENSP00000419422.1:n.-100C>A
NM_000685.4:c.-184C>A NP_000676.1:n.-184C>A
NM_004835.4:c.-53C>A NP_004826.5:n.-53C>A
NM_009585.3:c.-100C>A NP_033611.1:n.-100C>A
NM_031850.3:c.-137C>A NP_114038.4:n.-137C>A
NM_000685.5:c.-184C>A MANE Select NP_000676.1:n.-184C>A
NM_001382736.1:c.-122C>A NP_001369665.1:n.-122C>A
NM_001382737.1:c.-206C>A NP_001369666.1:n.-206C>A
NM_004835.5:c.-158C>A NP_004826.6:n.-158C>A
NM_009585.4:c.-100C>A NP_033611.1:n.-100C>A
NM_031850.4:c.-242C>A NP_114038.5:n.-242C>A
NM_032049.4:c.-315C>A NP_114438.3:n.-315C>A