Canonical Allele Identifier: CA2668116703

Gene: AGTR1

Linked Data

• gnomAD v4: 3-148742394-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742394C>A , CM000665.2:g.148742394C>A	GRCh38
NC_000003.11:g.148460181C>A , CM000665.1:g.148460181C>A	GRCh37
NC_000003.10:g.149942871C>A	NCBI36
NG_008468.1:g.49524C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*279C>A MANE Select	ENSP00000273430.3:n.*279C>A
ENST00000402260.2:c.*279C>A	ENSP00000385641.3:n.*279C>A
ENST00000418473.7:c.*279C>A	ENSP00000398832.4:n.*279C>A
ENST00000349243.7:c.*279C>A	ENSP00000273430.3:n.*279C>A
ENST00000402260.1:c.*279C>A	ENSP00000385641.2:n.*279C>A
ENST00000404754.2:c.*279C>A	ENSP00000385612.2:n.*279C>A
ENST00000418473.6:c.1464C>A	ENSP00000398832.3:n.1464C>A
ENST00000497524.5:c.*279C>A	ENSP00000419422.1:n.*279C>A
NM_000685.4:c.*279C>A	NP_000676.1:n.*279C>A
NM_004835.4:c.*279C>A	NP_004826.5:n.*279C>A
NM_009585.3:c.*279C>A	NP_033611.1:n.*279C>A
NM_031850.3:c.*279C>A	NP_114038.4:n.*279C>A
NM_032049.3:c.*279C>A	NP_114438.2:n.*279C>A
NM_000685.5:c.*279C>A MANE Select	NP_000676.1:n.*279C>A
NM_001382736.1:c.*279C>A	NP_001369665.1:n.*279C>A
NM_001382737.1:c.*279C>A	NP_001369666.1:n.*279C>A
NM_004835.5:c.*279C>A	NP_004826.6:n.*279C>A
NM_009585.4:c.*279C>A	NP_033611.1:n.*279C>A
NM_031850.4:c.*279C>A	NP_114038.5:n.*279C>A
NM_032049.4:c.*279C>A	NP_114438.3:n.*279C>A