Canonical Allele Identifier: CA900522215
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs1425854351

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148719982_148719997del , CM000665.2:g.148719982_148719997del GRCh38
NC_000003.11:g.148437769_148437784del , CM000665.1:g.148437769_148437784del GRCh37
NC_000003.10:g.149920459_149920474del NCBI36
NG_008468.1:g.27112_27127del

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-48+11955_-48+11970del MANE Select ENSP00000273430.3:n.-48+11955_-48+11970de...
ENST00000418473.7:c.-105-10198_-105-10183del ENSP00000398832.4:n.-105-10198_-105-10183...
ENST00000349243.7:c.-48+11955_-48+11970del ENSP00000273430.3:n.-48+11955_-48+11970de...
ENST00000404754.2:c.-47-21007_-47-20992del ENSP00000385612.2:n.-47-21007_-47-20992de...
ENST00000475166.5:n.217-10198_217-10183del
ENST00000497524.5:c.-47-21007_-47-20992del ENSP00000419422.1:n.-47-21007_-47-20992de...
NM_000685.4:c.-48+11955_-48+11970del NP_000676.1:n.-48+11955_-48+11970del
NM_004835.4:c.1-10198_1-10183del NP_004826.5:n.1-10198_1-10183del
NM_009585.3:c.-47-21007_-47-20992del NP_033611.1:n.-47-21007_-47-20992del
NM_031850.3:c.1-10198_1-10183del NP_114038.4:n.1-10198_1-10183del
NM_000685.5:c.-48+11955_-48+11970del MANE Select NP_000676.1:n.-48+11955_-48+11970del
NM_001382736.1:c.-47-21007_-47-20992del NP_001369665.1:n.-47-21007_-47-20992del
NM_001382737.1:c.-48+11955_-48+11970del NP_001369666.1:n.-48+11955_-48+11970del
NM_004835.5:c.-105-10198_-105-10183del NP_004826.6:n.-105-10198_-105-10183del
NM_009585.4:c.-47-21007_-47-20992del NP_033611.1:n.-47-21007_-47-20992del
NM_031850.4:c.-105-10198_-105-10183del NP_114038.5:n.-105-10198_-105-10183del
NM_032049.4:c.-262-10198_-262-10183del NP_114438.3:n.-262-10198_-262-10183del