Canonical Allele Identifier: CA2668116573
Gene: AGTR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148742041_148742044del , CM000665.2:g.148742041_148742044del GRCh38
NC_000003.11:g.148459828_148459831del , CM000665.1:g.148459828_148459831del GRCh37
NC_000003.10:g.149942518_149942521del NCBI36
NG_008468.1:g.49171_49174del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.1006_1009del MANE Select ENSP00000273430.3:p.Thr336PhefsTer9
ENST00000402260.2:c.1006_1009del ENSP00000385641.3:p.Thr336PhefsTer9
ENST00000418473.7:c.1006_1009del ENSP00000398832.4:p.Thr336PhefsTer9
ENST00000349243.7:c.1006_1009del ENSP00000273430.3:p.Thr336PhefsTer9
ENST00000402260.1:c.1093_1096del ENSP00000385641.2:p.Thr365PhefsTer9
ENST00000404754.2:c.1006_1009del ENSP00000385612.2:p.Thr336PhefsTer9
ENST00000418473.6:c.1111_1114del ENSP00000398832.3:p.Thr371PhefsTer9
ENST00000461609.1:c.1006_1009del ENSP00000418851.1:p.Thr336PhefsTer9
ENST00000474935.5:c.1006_1009del ENSP00000418084.1:p.Thr336PhefsTer9
ENST00000475347.5:c.1006_1009del ENSP00000419783.1:p.Thr336PhefsTer9
ENST00000497524.5:c.1006_1009del ENSP00000419422.1:p.Thr336PhefsTer9
NM_000685.4:c.1006_1009del NP_000676.1:p.Thr336PhefsTer9
NM_004835.4:c.1111_1114del NP_004826.5:p.Thr371PhefsTer9
NM_009585.3:c.1006_1009del NP_033611.1:p.Thr336PhefsTer9
NM_031850.3:c.1111_1114del NP_114038.4:p.Thr371PhefsTer9
NM_032049.3:c.1093_1096del NP_114438.2:p.Thr365PhefsTer9
NM_000685.5:c.1006_1009del MANE Select NP_000676.1:p.Thr336PhefsTer9
NM_001382736.1:c.1006_1009del NP_001369665.1:p.Thr336PhefsTer9
NM_001382737.1:c.1006_1009del NP_001369666.1:p.Thr336PhefsTer9
NM_004835.5:c.1006_1009del NP_004826.6:p.Thr336PhefsTer9
NM_009585.4:c.1006_1009del NP_033611.1:p.Thr336PhefsTer9
NM_031850.4:c.1006_1009del NP_114038.5:p.Thr336PhefsTer9
NM_032049.4:c.1006_1009del NP_114438.3:p.Thr336PhefsTer9