Canonical Allele Identifier: CA648255807

Gene: AGTR1

Linked Data

• COSMIC: COSN15623083

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742214_148742215insT , CM000665.2:g.148742214_148742215insT	GRCh38
NC_000003.11:g.148460001_148460002insT , CM000665.1:g.148460001_148460002insT	GRCh37
NC_000003.10:g.149942691_149942692insT	NCBI36
NG_008468.1:g.49344_49345insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*99_*100insT MANE Select	ENSP00000273430.3:n.*99_*100insT
ENST00000402260.2:c.*99_*100insT	ENSP00000385641.3:n.*99_*100insT
ENST00000418473.7:c.*99_*100insT	ENSP00000398832.4:n.*99_*100insT
ENST00000349243.7:c.*99_*100insT	ENSP00000273430.3:n.*99_*100insT
ENST00000402260.1:c.*99_*100insT	ENSP00000385641.2:n.*99_*100insT
ENST00000404754.2:c.*99_*100insT	ENSP00000385612.2:n.*99_*100insT
ENST00000418473.6:c.1284_1285insT	ENSP00000398832.3:n.1284_1285insT
ENST00000461609.1:c.*99_*100insT	ENSP00000418851.1:n.*99_*100insT
ENST00000474935.5:c.*99_*100insT	ENSP00000418084.1:n.*99_*100insT
ENST00000475347.5:c.*99_*100insT	ENSP00000419783.1:n.*99_*100insT
ENST00000497524.5:c.*99_*100insT	ENSP00000419422.1:n.*99_*100insT
NM_000685.4:c.*99_*100insT	NP_000676.1:n.*99_*100insT
NM_004835.4:c.*99_*100insT	NP_004826.5:n.*99_*100insT
NM_009585.3:c.*99_*100insT	NP_033611.1:n.*99_*100insT
NM_031850.3:c.*99_*100insT	NP_114038.4:n.*99_*100insT
NM_032049.3:c.*99_*100insT	NP_114438.2:n.*99_*100insT
NM_000685.5:c.*99_*100insT MANE Select	NP_000676.1:n.*99_*100insT
NM_001382736.1:c.*99_*100insT	NP_001369665.1:n.*99_*100insT
NM_001382737.1:c.*99_*100insT	NP_001369666.1:n.*99_*100insT
NM_004835.5:c.*99_*100insT	NP_004826.6:n.*99_*100insT
NM_009585.4:c.*99_*100insT	NP_033611.1:n.*99_*100insT
NM_031850.4:c.*99_*100insT	NP_114038.5:n.*99_*100insT
NM_032049.4:c.*99_*100insT	NP_114438.3:n.*99_*100insT