Canonical Allele Identifier: CA85562160

Gene: AGTR1

Linked Data

• dbSNP Id: rs527725239
• gnomAD v2: 3-148426527-GTCCGGGATT-G
• gnomAD v3: 3-148708740-GTCCGGGATT-G
• gnomAD v4: 3-148708740-GTCCGGGATT-G
• MyVariant Identifiers: chr3:g.148426528_148426536del (hg19) ; chr3:g.148708741_148708749del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708742_148708750del , CM000665.2:g.148708742_148708750del	GRCh38
NC_000003.11:g.148426529_148426537del , CM000665.1:g.148426529_148426537del	GRCh37
NC_000003.10:g.149909219_149909227del	NCBI36
NG_008468.1:g.15872_15880del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+715_-48+723del MANE Select	ENSP00000273430.3:n.-48+715_-48+723del
ENST00000418473.7:c.-106+10615_-106+10623del	ENSP00000398832.4:n.-106+10615_-106+10623del
ENST00000349243.7:c.-48+715_-48+723del	ENSP00000273430.3:n.-48+715_-48+723del
ENST00000404754.2:c.-48+10593_-48+10601del	ENSP00000385612.2:n.-48+10593_-48+10601del
ENST00000475166.5:n.216+715_216+723del
ENST00000497524.5:c.-48+10615_-48+10623del	ENSP00000419422.1:n.-48+10615_-48+10623del
NM_000685.4:c.-48+715_-48+723del	NP_000676.1:n.-48+715_-48+723del
NM_004835.4:c.-1+10615_-1+10623del	NP_004826.5:n.-1+10615_-1+10623del
NM_009585.3:c.-48+10615_-48+10623del	NP_033611.1:n.-48+10615_-48+10623del
NM_031850.3:c.-1+715_-1+723del	NP_114038.4:n.-1+715_-1+723del
NM_000685.5:c.-48+715_-48+723del MANE Select	NP_000676.1:n.-48+715_-48+723del
NM_001382736.1:c.-48+10593_-48+10601del	NP_001369665.1:n.-48+10593_-48+10601del
NM_001382737.1:c.-48+715_-48+723del	NP_001369666.1:n.-48+715_-48+723del
NM_004835.5:c.-106+10615_-106+10623del	NP_004826.6:n.-106+10615_-106+10623del
NM_009585.4:c.-48+10615_-48+10623del	NP_033611.1:n.-48+10615_-48+10623del
NM_031850.4:c.-106+715_-106+723del	NP_114038.5:n.-106+715_-106+723del
NM_032049.4:c.-263+10615_-263+10623del	NP_114438.3:n.-263+10615_-263+10623del