Canonical Allele Identifier: CA1139658298

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148707960A>G , CM000665.2:g.148707960A>G	GRCh38
NC_000003.11:g.148425747A>G , CM000665.1:g.148425747A>G	GRCh37
NC_000003.10:g.149908437A>G	NCBI36
NG_008468.1:g.15090A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-115A>G MANE Select	ENSP00000273430.3:n.-115A>G
ENST00000418473.7:c.-106+9833A>G	ENSP00000398832.4:n.-106+9833A>G
ENST00000349243.7:c.-115A>G	ENSP00000273430.3:n.-115A>G
ENST00000404754.2:c.-48+9811A>G	ENSP00000385612.2:n.-48+9811A>G
ENST00000475166.5:n.149A>G
ENST00000497524.5:c.-48+9833A>G	ENSP00000419422.1:n.-48+9833A>G
NM_000685.4:c.-115A>G	NP_000676.1:n.-115A>G
NM_004835.4:c.-1+9833A>G	NP_004826.5:n.-1+9833A>G
NM_009585.3:c.-48+9833A>G	NP_033611.1:n.-48+9833A>G
NM_031850.3:c.-68A>G	NP_114038.4:n.-68A>G
NM_000685.5:c.-115A>G MANE Select	NP_000676.1:n.-115A>G
NM_001382736.1:c.-48+9811A>G	NP_001369665.1:n.-48+9811A>G
NM_001382737.1:c.-115A>G	NP_001369666.1:n.-115A>G
NM_004835.5:c.-106+9833A>G	NP_004826.6:n.-106+9833A>G
NM_009585.4:c.-48+9833A>G	NP_033611.1:n.-48+9833A>G
NM_031850.4:c.-173A>G	NP_114038.5:n.-173A>G
NM_032049.4:c.-263+9833A>G	NP_114438.3:n.-263+9833A>G