Canonical Allele Identifier: CA1409909810

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741542_148741544delinsATT , CM000665.2:g.148741542_148741544delinsATT	GRCh38
NC_000003.11:g.148459329_148459331delinsATT , CM000665.1:g.148459329_148459331delinsATT	GRCh37
NC_000003.10:g.149942019_149942021delinsATT	NCBI36
NG_008468.1:g.48672_48674delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.507_509delinsATT MANE Select	ENSP00000273430.3:p.Val169=
ENST00000402260.2:c.507_509delinsATT	ENSP00000385641.3:p.Val169=
ENST00000418473.7:c.507_509delinsATT	ENSP00000398832.4:p.Val169=
ENST00000349243.7:c.507_509delinsATT	ENSP00000273430.3:p.Val169=
ENST00000402260.1:c.594_596delinsATT	ENSP00000385641.2:p.Val198=
ENST00000404754.2:c.507_509delinsATT	ENSP00000385612.2:p.Val169=
ENST00000418473.6:c.612_614delinsATT	ENSP00000398832.3:p.Val204=
ENST00000461609.1:c.507_509delinsATT	ENSP00000418851.1:p.Val169=
ENST00000474935.5:c.507_509delinsATT	ENSP00000418084.1:p.Val169=
ENST00000475347.5:c.507_509delinsATT	ENSP00000419783.1:p.Val169=
ENST00000497524.5:c.507_509delinsATT	ENSP00000419422.1:p.Val169=
NM_000685.4:c.507_509delinsATT	NP_000676.1:p.Val169=
NM_004835.4:c.612_614delinsATT	NP_004826.5:p.Val204=
NM_009585.3:c.507_509delinsATT	NP_033611.1:p.Val169=
NM_031850.3:c.612_614delinsATT	NP_114038.4:p.Val204=
NM_032049.3:c.594_596delinsATT	NP_114438.2:p.Val198=
NM_000685.5:c.507_509delinsATT MANE Select	NP_000676.1:p.Val169=
NM_001382736.1:c.507_509delinsATT	NP_001369665.1:p.Val169=
NM_001382737.1:c.507_509delinsATT	NP_001369666.1:p.Val169=
NM_004835.5:c.507_509delinsATT	NP_004826.6:p.Val169=
NM_009585.4:c.507_509delinsATT	NP_033611.1:p.Val169=
NM_031850.4:c.507_509delinsATT	NP_114038.5:p.Val169=
NM_032049.4:c.507_509delinsATT	NP_114438.3:p.Val169=