Canonical Allele Identifier: CA1409900569

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148712505_148712506delinsAG , CM000665.2:g.148712505_148712506delinsAG	GRCh38
NC_000003.11:g.148430292_148430293delinsAG , CM000665.1:g.148430292_148430293delinsAG	GRCh37
NC_000003.10:g.149912982_149912983delinsAG	NCBI36
NG_008468.1:g.19635_19636delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000349243.8:c.-48+4478_-48+4479delinsAG MANE Select	ENSP00000273430.3:n.-48+4478_-48+4479deli...
ENST00000418473.7:c.-106+14378_-106+14379delinsAG	ENSP00000398832.4:n.-106+14378_-106+14379...
ENST00000349243.7:c.-48+4478_-48+4479delinsAG	ENSP00000273430.3:n.-48+4478_-48+4479deli...
ENST00000404754.2:c.-48+14356_-48+14357delinsAG	ENSP00000385612.2:n.-48+14356_-48+14357de...
ENST00000475166.5:n.216+4478_216+4479delinsAG
ENST00000497524.5:c.-48+14378_-48+14379delinsAG	ENSP00000419422.1:n.-48+14378_-48+14379de...
NM_000685.4:c.-48+4478_-48+4479delinsAG	NP_000676.1:n.-48+4478_-48+4479delinsAG
NM_004835.4:c.-1+14378_-1+14379delinsAG	NP_004826.5:n.-1+14378_-1+14379delinsAG
NM_009585.3:c.-48+14378_-48+14379delinsAG	NP_033611.1:n.-48+14378_-48+14379delinsAG...
NM_031850.3:c.-1+4478_-1+4479delinsAG	NP_114038.4:n.-1+4478_-1+4479delinsAG
NM_000685.5:c.-48+4478_-48+4479delinsAG MANE Select	NP_000676.1:n.-48+4478_-48+4479delinsAG
NM_001382736.1:c.-48+14356_-48+14357delinsAG	NP_001369665.1:n.-48+14356_-48+14357delin...
NM_001382737.1:c.-48+4478_-48+4479delinsAG	NP_001369666.1:n.-48+4478_-48+4479delinsA...
NM_004835.5:c.-106+14378_-106+14379delinsAG	NP_004826.6:n.-106+14378_-106+14379delins...
NM_009585.4:c.-48+14378_-48+14379delinsAG	NP_033611.1:n.-48+14378_-48+14379delinsAG...
NM_031850.4:c.-106+4478_-106+4479delinsAG	NP_114038.5:n.-106+4478_-106+4479delinsAG...
NM_032049.4:c.-263+14378_-263+14379delinsAG	NP_114438.3:n.-263+14378_-263+14379delins...