Canonical Allele Identifier: CA648255786

Gene: AGTR1

Linked Data

• COSMIC: COSN18728549

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742156_148742157insT , CM000665.2:g.148742156_148742157insT	GRCh38
NC_000003.11:g.148459943_148459944insT , CM000665.1:g.148459943_148459944insT	GRCh37
NC_000003.10:g.149942633_149942634insT	NCBI36
NG_008468.1:g.49286_49287insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*41_*42insT MANE Select	ENSP00000273430.3:n.*41_*42insT
ENST00000402260.2:c.*41_*42insT	ENSP00000385641.3:n.*41_*42insT
ENST00000418473.7:c.*41_*42insT	ENSP00000398832.4:n.*41_*42insT
ENST00000349243.7:c.*41_*42insT	ENSP00000273430.3:n.*41_*42insT
ENST00000402260.1:c.*41_*42insT	ENSP00000385641.2:n.*41_*42insT
ENST00000404754.2:c.*41_*42insT	ENSP00000385612.2:n.*41_*42insT
ENST00000418473.6:c.1226_1227insT	ENSP00000398832.3:n.1226_1227insT
ENST00000461609.1:c.*41_*42insT	ENSP00000418851.1:n.*41_*42insT
ENST00000474935.5:c.*41_*42insT	ENSP00000418084.1:n.*41_*42insT
ENST00000475347.5:c.*41_*42insT	ENSP00000419783.1:n.*41_*42insT
ENST00000497524.5:c.*41_*42insT	ENSP00000419422.1:n.*41_*42insT
NM_000685.4:c.*41_*42insT	NP_000676.1:n.*41_*42insT
NM_004835.4:c.*41_*42insT	NP_004826.5:n.*41_*42insT
NM_009585.3:c.*41_*42insT	NP_033611.1:n.*41_*42insT
NM_031850.3:c.*41_*42insT	NP_114038.4:n.*41_*42insT
NM_032049.3:c.*41_*42insT	NP_114438.2:n.*41_*42insT
NM_000685.5:c.*41_*42insT MANE Select	NP_000676.1:n.*41_*42insT
NM_001382736.1:c.*41_*42insT	NP_001369665.1:n.*41_*42insT
NM_001382737.1:c.*41_*42insT	NP_001369666.1:n.*41_*42insT
NM_004835.5:c.*41_*42insT	NP_004826.6:n.*41_*42insT
NM_009585.4:c.*41_*42insT	NP_033611.1:n.*41_*42insT
NM_031850.4:c.*41_*42insT	NP_114038.5:n.*41_*42insT
NM_032049.4:c.*41_*42insT	NP_114438.3:n.*41_*42insT