Canonical Allele Identifier: CA2522998680

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708686_148708687insAAGG , CM000665.2:g.148708686_148708687insAAGG	GRCh38
NC_000003.11:g.148426473_148426474insAAGG , CM000665.1:g.148426473_148426474insAAGG	GRCh37
NC_000003.10:g.149909163_149909164insAAGG	NCBI36
NG_008468.1:g.15816_15817insAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+659_-48+660insAAGG MANE Select	ENSP00000273430.3:n.-48+659_-48+660insAAGG
ENST00000418473.7:c.-106+10559_-106+10560insAAGG	ENSP00000398832.4:n.-106+10559_-106+10560insAAGG
ENST00000349243.7:c.-48+659_-48+660insAAGG	ENSP00000273430.3:n.-48+659_-48+660insAAGG
ENST00000404754.2:c.-48+10537_-48+10538insAAGG	ENSP00000385612.2:n.-48+10537_-48+10538insAAGG
ENST00000475166.5:n.216+659_216+660insAAGG
ENST00000497524.5:c.-48+10559_-48+10560insAAGG	ENSP00000419422.1:n.-48+10559_-48+10560insAAGG
NM_000685.4:c.-48+659_-48+660insAAGG	NP_000676.1:n.-48+659_-48+660insAAGG
NM_004835.4:c.-1+10559_-1+10560insAAGG	NP_004826.5:n.-1+10559_-1+10560insAAGG
NM_009585.3:c.-48+10559_-48+10560insAAGG	NP_033611.1:n.-48+10559_-48+10560insAAGG
NM_031850.3:c.-1+659_-1+660insAAGG	NP_114038.4:n.-1+659_-1+660insAAGG
NM_000685.5:c.-48+659_-48+660insAAGG MANE Select	NP_000676.1:n.-48+659_-48+660insAAGG
NM_001382736.1:c.-48+10537_-48+10538insAAGG	NP_001369665.1:n.-48+10537_-48+10538insAAGG
NM_001382737.1:c.-48+659_-48+660insAAGG	NP_001369666.1:n.-48+659_-48+660insAAGG
NM_004835.5:c.-106+10559_-106+10560insAAGG	NP_004826.6:n.-106+10559_-106+10560insAAGG
NM_009585.4:c.-48+10559_-48+10560insAAGG	NP_033611.1:n.-48+10559_-48+10560insAAGG
NM_031850.4:c.-106+659_-106+660insAAGG	NP_114038.5:n.-106+659_-106+660insAAGG
NM_032049.4:c.-263+10559_-263+10560insAAGG	NP_114438.3:n.-263+10559_-263+10560insAAGG