Canonical Allele Identifier: CA354888478

Gene: AGTR1

Linked Data

• COSMIC: COSM6054119
• MyVariant Identifiers: chr3:g.148459477T>C (hg19) ; chr3:g.148741690T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741690T>C , CM000665.2:g.148741690T>C	GRCh38
NC_000003.11:g.148459477T>C , CM000665.1:g.148459477T>C	GRCh37
NC_000003.10:g.149942167T>C	NCBI36
NG_008468.1:g.48820T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.655T>C MANE Select	ENSP00000273430.3:p.Trp219Arg
ENST00000402260.2:c.655T>C	ENSP00000385641.3:p.Trp219Arg
ENST00000418473.7:c.655T>C	ENSP00000398832.4:p.Trp219Arg
ENST00000349243.7:c.655T>C	ENSP00000273430.3:p.Trp219Arg
ENST00000402260.1:c.742T>C	ENSP00000385641.2:p.Trp248Arg
ENST00000404754.2:c.655T>C	ENSP00000385612.2:p.Trp219Arg
ENST00000418473.6:c.760T>C	ENSP00000398832.3:p.Trp254Arg
ENST00000461609.1:c.655T>C	ENSP00000418851.1:p.Trp219Arg
ENST00000474935.5:c.655T>C	ENSP00000418084.1:p.Trp219Arg
ENST00000475347.5:c.655T>C	ENSP00000419783.1:p.Trp219Arg
ENST00000497524.5:c.655T>C	ENSP00000419422.1:p.Trp219Arg
NM_000685.4:c.655T>C	NP_000676.1:p.Trp219Arg
NM_004835.4:c.760T>C	NP_004826.5:p.Trp254Arg
NM_009585.3:c.655T>C	NP_033611.1:p.Trp219Arg
NM_031850.3:c.760T>C	NP_114038.4:p.Trp254Arg
NM_032049.3:c.742T>C	NP_114438.2:p.Trp248Arg
NM_000685.5:c.655T>C MANE Select	NP_000676.1:p.Trp219Arg
NM_001382736.1:c.655T>C	NP_001369665.1:p.Trp219Arg
NM_001382737.1:c.655T>C	NP_001369666.1:p.Trp219Arg
NM_004835.5:c.655T>C	NP_004826.6:p.Trp219Arg
NM_009585.4:c.655T>C	NP_033611.1:p.Trp219Arg
NM_031850.4:c.655T>C	NP_114038.5:p.Trp219Arg
NM_032049.4:c.655T>C	NP_114438.3:p.Trp219Arg