Canonical Allele Identifier: CA2546719914

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708688_148708689insTATG , CM000665.2:g.148708688_148708689insTATG	GRCh38
NC_000003.11:g.148426475_148426476insTATG , CM000665.1:g.148426475_148426476insTATG	GRCh37
NC_000003.10:g.149909165_149909166insTATG	NCBI36
NG_008468.1:g.15818_15819insTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+661_-48+662insTATG MANE Select	ENSP00000273430.3:n.-48+661_-48+662insTATG
ENST00000418473.7:c.-106+10561_-106+10562insTATG	ENSP00000398832.4:n.-106+10561_-106+10562insTATG
ENST00000349243.7:c.-48+661_-48+662insTATG	ENSP00000273430.3:n.-48+661_-48+662insTATG
ENST00000404754.2:c.-48+10539_-48+10540insTATG	ENSP00000385612.2:n.-48+10539_-48+10540insTATG
ENST00000475166.5:n.216+661_216+662insTATG
ENST00000497524.5:c.-48+10561_-48+10562insTATG	ENSP00000419422.1:n.-48+10561_-48+10562insTATG
NM_000685.4:c.-48+661_-48+662insTATG	NP_000676.1:n.-48+661_-48+662insTATG
NM_004835.4:c.-1+10561_-1+10562insTATG	NP_004826.5:n.-1+10561_-1+10562insTATG
NM_009585.3:c.-48+10561_-48+10562insTATG	NP_033611.1:n.-48+10561_-48+10562insTATG
NM_031850.3:c.-1+661_-1+662insTATG	NP_114038.4:n.-1+661_-1+662insTATG
NM_000685.5:c.-48+661_-48+662insTATG MANE Select	NP_000676.1:n.-48+661_-48+662insTATG
NM_001382736.1:c.-48+10539_-48+10540insTATG	NP_001369665.1:n.-48+10539_-48+10540insTATG
NM_001382737.1:c.-48+661_-48+662insTATG	NP_001369666.1:n.-48+661_-48+662insTATG
NM_004835.5:c.-106+10561_-106+10562insTATG	NP_004826.6:n.-106+10561_-106+10562insTATG
NM_009585.4:c.-48+10561_-48+10562insTATG	NP_033611.1:n.-48+10561_-48+10562insTATG
NM_031850.4:c.-106+661_-106+662insTATG	NP_114038.5:n.-106+661_-106+662insTATG
NM_032049.4:c.-263+10561_-263+10562insTATG	NP_114438.3:n.-263+10561_-263+10562insTATG