Canonical Allele Identifier: CA917033409

Gene: AGTR1

Linked Data

• dbSNP Id: rs1576525029

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708763_148708765del , CM000665.2:g.148708763_148708765del	GRCh38
NC_000003.11:g.148426550_148426552del , CM000665.1:g.148426550_148426552del	GRCh37
NC_000003.10:g.149909240_149909242del	NCBI36
NG_008468.1:g.15893_15895del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+736_-48+738del MANE Select	ENSP00000273430.3:n.-48+736_-48+738del
ENST00000418473.7:c.-106+10636_-106+10638del	ENSP00000398832.4:n.-106+10636_-106+10638del
ENST00000349243.7:c.-48+736_-48+738del	ENSP00000273430.3:n.-48+736_-48+738del
ENST00000404754.2:c.-48+10614_-48+10616del	ENSP00000385612.2:n.-48+10614_-48+10616del
ENST00000475166.5:n.216+736_216+738del
ENST00000497524.5:c.-48+10636_-48+10638del	ENSP00000419422.1:n.-48+10636_-48+10638del
NM_000685.4:c.-48+736_-48+738del	NP_000676.1:n.-48+736_-48+738del
NM_004835.4:c.-1+10636_-1+10638del	NP_004826.5:n.-1+10636_-1+10638del
NM_009585.3:c.-48+10636_-48+10638del	NP_033611.1:n.-48+10636_-48+10638del
NM_031850.3:c.-1+736_-1+738del	NP_114038.4:n.-1+736_-1+738del
NM_000685.5:c.-48+736_-48+738del MANE Select	NP_000676.1:n.-48+736_-48+738del
NM_001382736.1:c.-48+10614_-48+10616del	NP_001369665.1:n.-48+10614_-48+10616del
NM_001382737.1:c.-48+736_-48+738del	NP_001369666.1:n.-48+736_-48+738del
NM_004835.5:c.-106+10636_-106+10638del	NP_004826.6:n.-106+10636_-106+10638del
NM_009585.4:c.-48+10636_-48+10638del	NP_033611.1:n.-48+10636_-48+10638del
NM_031850.4:c.-106+736_-106+738del	NP_114038.5:n.-106+736_-106+738del
NM_032049.4:c.-263+10636_-263+10638del	NP_114438.3:n.-263+10636_-263+10638del