Canonical Allele Identifier: CA1409899066

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708740_148708749delinsGTCCGGGATT , CM000665.2:g.148708740_148708749delinsGTCCGGGATT	GRCh38
NC_000003.11:g.148426527_148426536delinsGTCCGGGATT , CM000665.1:g.148426527_148426536delinsGTCCGGGATT	GRCh37
NC_000003.10:g.149909217_149909226delinsGTCCGGGATT	NCBI36
NG_008468.1:g.15870_15879delinsGTCCGGGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+713_-48+722delinsGTCCGGGATT MANE Select	ENSP00000273430.3:n.-48+713_-48+722delinsGTCCGGGATT
ENST00000418473.7:c.-106+10613_-106+10622delinsGTCCGGGATT	ENSP00000398832.4:n.-106+10613_-106+10622delinsGTCCGGGATT
ENST00000349243.7:c.-48+713_-48+722delinsGTCCGGGATT	ENSP00000273430.3:n.-48+713_-48+722delinsGTCCGGGATT
ENST00000404754.2:c.-48+10591_-48+10600delinsGTCCGGGATT	ENSP00000385612.2:n.-48+10591_-48+10600delinsGTCCGGGATT
ENST00000475166.5:n.216+713_216+722delinsGTCCGGGATT
ENST00000497524.5:c.-48+10613_-48+10622delinsGTCCGGGATT	ENSP00000419422.1:n.-48+10613_-48+10622delinsGTCCGGGATT
NM_000685.4:c.-48+713_-48+722delinsGTCCGGGATT	NP_000676.1:n.-48+713_-48+722delinsGTCCGGGATT
NM_004835.4:c.-1+10613_-1+10622delinsGTCCGGGATT	NP_004826.5:n.-1+10613_-1+10622delinsGTCCGGGATT
NM_009585.3:c.-48+10613_-48+10622delinsGTCCGGGATT	NP_033611.1:n.-48+10613_-48+10622delinsGTCCGGGATT
NM_031850.3:c.-1+713_-1+722delinsGTCCGGGATT	NP_114038.4:n.-1+713_-1+722delinsGTCCGGGATT
NM_000685.5:c.-48+713_-48+722delinsGTCCGGGATT MANE Select	NP_000676.1:n.-48+713_-48+722delinsGTCCGGGATT
NM_001382736.1:c.-48+10591_-48+10600delinsGTCCGGGATT	NP_001369665.1:n.-48+10591_-48+10600delinsGTCCGGGATT
NM_001382737.1:c.-48+713_-48+722delinsGTCCGGGATT	NP_001369666.1:n.-48+713_-48+722delinsGTCCGGGATT
NM_004835.5:c.-106+10613_-106+10622delinsGTCCGGGATT	NP_004826.6:n.-106+10613_-106+10622delinsGTCCGGGATT
NM_009585.4:c.-48+10613_-48+10622delinsGTCCGGGATT	NP_033611.1:n.-48+10613_-48+10622delinsGTCCGGGATT
NM_031850.4:c.-106+713_-106+722delinsGTCCGGGATT	NP_114038.5:n.-106+713_-106+722delinsGTCCGGGATT
NM_032049.4:c.-263+10613_-263+10622delinsGTCCGGGATT	NP_114438.3:n.-263+10613_-263+10622delinsGTCCGGGATT