Canonical Allele Identifier: CA645531657

Gene: AGTR1

Linked Data

• COSMIC: COSM308996

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742042_148742043delinsTT , CM000665.2:g.148742042_148742043delinsTT	GRCh38
NC_000003.11:g.148459829_148459830delinsTT , CM000665.1:g.148459829_148459830delinsTT	GRCh37
NC_000003.10:g.149942519_149942520delinsTT	NCBI36
NG_008468.1:g.49172_49173delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.1007_1008delinsTT MANE Select	ENSP00000273430.3:p.Thr336Ile
ENST00000402260.2:c.1007_1008delinsTT	ENSP00000385641.3:p.Thr336Ile
ENST00000418473.7:c.1007_1008delinsTT	ENSP00000398832.4:p.Thr336Ile
ENST00000349243.7:c.1007_1008delinsTT	ENSP00000273430.3:p.Thr336Ile
ENST00000402260.1:c.1094_1095delinsTT	ENSP00000385641.2:p.Thr365Ile
ENST00000404754.2:c.1007_1008delinsTT	ENSP00000385612.2:p.Thr336Ile
ENST00000418473.6:c.1112_1113delinsTT	ENSP00000398832.3:p.Thr371Ile
ENST00000461609.1:c.1007_1008delinsTT	ENSP00000418851.1:p.Thr336Ile
ENST00000474935.5:c.1007_1008delinsTT	ENSP00000418084.1:p.Thr336Ile
ENST00000475347.5:c.1007_1008delinsTT	ENSP00000419783.1:p.Thr336Ile
ENST00000497524.5:c.1007_1008delinsTT	ENSP00000419422.1:p.Thr336Ile
NM_000685.4:c.1007_1008delinsTT	NP_000676.1:p.Thr336Ile
NM_004835.4:c.1112_1113delinsTT	NP_004826.5:p.Thr371Ile
NM_009585.3:c.1007_1008delinsTT	NP_033611.1:p.Thr336Ile
NM_031850.3:c.1112_1113delinsTT	NP_114038.4:p.Thr371Ile
NM_032049.3:c.1094_1095delinsTT	NP_114438.2:p.Thr365Ile
NM_000685.5:c.1007_1008delinsTT MANE Select	NP_000676.1:p.Thr336Ile
NM_001382736.1:c.1007_1008delinsTT	NP_001369665.1:p.Thr336Ile
NM_001382737.1:c.1007_1008delinsTT	NP_001369666.1:p.Thr336Ile
NM_004835.5:c.1007_1008delinsTT	NP_004826.6:p.Thr336Ile
NM_009585.4:c.1007_1008delinsTT	NP_033611.1:p.Thr336Ile
NM_031850.4:c.1007_1008delinsTT	NP_114038.5:p.Thr336Ile
NM_032049.4:c.1007_1008delinsTT	NP_114438.3:p.Thr336Ile