Canonical Allele Identifier: CA10617450
Gene: AGTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148742432G>A , CM000665.2:g.148742432G>A GRCh38
NC_000003.11:g.148460219G>A , CM000665.1:g.148460219G>A GRCh37
NC_000003.10:g.149942909G>A NCBI36
NG_008468.1:g.49562G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.*317G>A MANE Select ENSP00000273430.3:n.*317G>A
ENST00000402260.2:c.*317G>A ENSP00000385641.3:n.*317G>A
ENST00000418473.7:c.*317G>A ENSP00000398832.4:n.*317G>A
ENST00000349243.7:c.*317G>A ENSP00000273430.3:n.*317G>A
ENST00000402260.1:c.*317G>A ENSP00000385641.2:n.*317G>A
ENST00000404754.2:c.*317G>A ENSP00000385612.2:n.*317G>A
ENST00000418473.6:c.1502G>A ENSP00000398832.3:n.1502G>A
ENST00000497524.5:c.*317G>A ENSP00000419422.1:n.*317G>A
NM_000685.4:c.*317G>A NP_000676.1:n.*317G>A
NM_004835.4:c.*317G>A NP_004826.5:n.*317G>A
NM_009585.3:c.*317G>A NP_033611.1:n.*317G>A
NM_031850.3:c.*317G>A NP_114038.4:n.*317G>A
NM_032049.3:c.*317G>A NP_114438.2:n.*317G>A
NM_000685.5:c.*317G>A MANE Select NP_000676.1:n.*317G>A
NM_001382736.1:c.*317G>A NP_001369665.1:n.*317G>A
NM_001382737.1:c.*317G>A NP_001369666.1:n.*317G>A
NM_004835.5:c.*317G>A NP_004826.6:n.*317G>A
NM_009585.4:c.*317G>A NP_033611.1:n.*317G>A
NM_031850.4:c.*317G>A NP_114038.5:n.*317G>A
NM_032049.4:c.*317G>A NP_114438.3:n.*317G>A