Canonical Allele Identifier: CA1409899059

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708728T= , CM000665.2:g.148708728T=	GRCh38
NC_000003.11:g.148426515T= , CM000665.1:g.148426515T=	GRCh37
NC_000003.10:g.149909205T=	NCBI36
NG_008468.1:g.15858T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+701T= MANE Select	ENSP00000273430.3:n.-48+701T=
ENST00000418473.7:c.-106+10601T=	ENSP00000398832.4:n.-106+10601T=
ENST00000349243.7:c.-48+701T=	ENSP00000273430.3:n.-48+701T=
ENST00000404754.2:c.-48+10579T=	ENSP00000385612.2:n.-48+10579T=
ENST00000475166.5:n.216+701T=
ENST00000497524.5:c.-48+10601T=	ENSP00000419422.1:n.-48+10601T=
NM_000685.4:c.-48+701T=	NP_000676.1:n.-48+701T=
NM_004835.4:c.-1+10601T=	NP_004826.5:n.-1+10601T=
NM_009585.3:c.-48+10601T=	NP_033611.1:n.-48+10601T=
NM_031850.3:c.-1+701T=	NP_114038.4:n.-1+701T=
NM_000685.5:c.-48+701T= MANE Select	NP_000676.1:n.-48+701T=
NM_001382736.1:c.-48+10579T=	NP_001369665.1:n.-48+10579T=
NM_001382737.1:c.-48+701T=	NP_001369666.1:n.-48+701T=
NM_004835.5:c.-106+10601T=	NP_004826.6:n.-106+10601T=
NM_009585.4:c.-48+10601T=	NP_033611.1:n.-48+10601T=
NM_031850.4:c.-106+701T=	NP_114038.5:n.-106+701T=
NM_032049.4:c.-263+10601T=	NP_114438.3:n.-263+10601T=