Canonical Allele Identifier: CA1409910459
Gene: AGTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148742000_148742001delinsCA , CM000665.2:g.148742000_148742001delinsCA GRCh38
NC_000003.11:g.148459787_148459788delinsCA , CM000665.1:g.148459787_148459788delinsCA GRCh37
NC_000003.10:g.149942477_149942478delinsCA NCBI36
NG_008468.1:g.49130_49131delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.965_966delinsCA MANE Select ENSP00000273430.3:p.Pro322=
ENST00000402260.2:c.965_966delinsCA ENSP00000385641.3:p.Pro322=
ENST00000418473.7:c.965_966delinsCA ENSP00000398832.4:p.Pro322=
ENST00000349243.7:c.965_966delinsCA ENSP00000273430.3:p.Pro322=
ENST00000402260.1:c.1052_1053delinsCA ENSP00000385641.2:p.Pro351=
ENST00000404754.2:c.965_966delinsCA ENSP00000385612.2:p.Pro322=
ENST00000418473.6:c.1070_1071delinsCA ENSP00000398832.3:p.Pro357=
ENST00000461609.1:c.965_966delinsCA ENSP00000418851.1:p.Pro322=
ENST00000474935.5:c.965_966delinsCA ENSP00000418084.1:p.Pro322=
ENST00000475347.5:c.965_966delinsCA ENSP00000419783.1:p.Pro322=
ENST00000497524.5:c.965_966delinsCA ENSP00000419422.1:p.Pro322=
NM_000685.4:c.965_966delinsCA NP_000676.1:p.Pro322=
NM_004835.4:c.1070_1071delinsCA NP_004826.5:p.Pro357=
NM_009585.3:c.965_966delinsCA NP_033611.1:p.Pro322=
NM_031850.3:c.1070_1071delinsCA NP_114038.4:p.Pro357=
NM_032049.3:c.1052_1053delinsCA NP_114438.2:p.Pro351=
NM_000685.5:c.965_966delinsCA MANE Select NP_000676.1:p.Pro322=
NM_001382736.1:c.965_966delinsCA NP_001369665.1:p.Pro322=
NM_001382737.1:c.965_966delinsCA NP_001369666.1:p.Pro322=
NM_004835.5:c.965_966delinsCA NP_004826.6:p.Pro322=
NM_009585.4:c.965_966delinsCA NP_033611.1:p.Pro322=
NM_031850.4:c.965_966delinsCA NP_114038.5:p.Pro322=
NM_032049.4:c.965_966delinsCA NP_114438.3:p.Pro322=