Canonical Allele Identifier: CA2657435
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs753563079

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148742081_148742083del , CM000665.2:g.148742081_148742083del GRCh38
NC_000003.11:g.148459868_148459870del , CM000665.1:g.148459868_148459870del GRCh37
NC_000003.10:g.149942558_149942560del NCBI36
NG_008468.1:g.49211_49213del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.1046_1048del MANE Select ENSP00000273430.3:p.Thr349del
ENST00000402260.2:c.1046_1048del ENSP00000385641.3:p.Thr349del
ENST00000418473.7:c.1046_1048del ENSP00000398832.4:p.Thr349del
ENST00000349243.7:c.1046_1048del ENSP00000273430.3:p.Thr349del
ENST00000402260.1:c.1133_1135del ENSP00000385641.2:p.Thr378del
ENST00000404754.2:c.1046_1048del ENSP00000385612.2:p.Thr349del
ENST00000418473.6:c.1151_1153del ENSP00000398832.3:p.Thr384del
ENST00000461609.1:c.1046_1048del ENSP00000418851.1:p.Thr349del
ENST00000474935.5:c.1046_1048del ENSP00000418084.1:p.Thr349del
ENST00000475347.5:c.1046_1048del ENSP00000419783.1:p.Thr349del
ENST00000497524.5:c.1046_1048del ENSP00000419422.1:p.Thr349del
NM_000685.4:c.1046_1048del NP_000676.1:p.Thr349del
NM_004835.4:c.1151_1153del NP_004826.5:p.Thr384del
NM_009585.3:c.1046_1048del NP_033611.1:p.Thr349del
NM_031850.3:c.1151_1153del NP_114038.4:p.Thr384del
NM_032049.3:c.1133_1135del NP_114438.2:p.Thr378del
NM_000685.5:c.1046_1048del MANE Select NP_000676.1:p.Thr349del
NM_001382736.1:c.1046_1048del NP_001369665.1:p.Thr349del
NM_001382737.1:c.1046_1048del NP_001369666.1:p.Thr349del
NM_004835.5:c.1046_1048del NP_004826.6:p.Thr349del
NM_009585.4:c.1046_1048del NP_033611.1:p.Thr349del
NM_031850.4:c.1046_1048del NP_114038.5:p.Thr349del
NM_032049.4:c.1046_1048del NP_114438.3:p.Thr349del