Canonical Allele Identifier: CA85569632

Gene: AGTR1

Linked Data

• dbSNP Id: rs770605989
• gnomAD v3: 3-148725390-GTAT-G
• gnomAD v4: 3-148725390-GTAT-G
• MyVariant Identifiers: chr3:g.148443178_148443180del (hg19) ; chr3:g.148725391_148725393del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148725396_148725398del , CM000665.2:g.148725396_148725398del	GRCh38
NC_000003.11:g.148443183_148443185del , CM000665.1:g.148443183_148443185del	GRCh37
NC_000003.10:g.149925873_149925875del	NCBI36
NG_008468.1:g.32526_32528del

Transcript Alleles

HGVS	Amino-acid change
ENST00000349243.8:c.-47-15593_-47-15591del MANE Select	ENSP00000273430.3:n.-47-15593_-47-15591de...
ENST00000418473.7:c.-105-4784_-105-4782del	ENSP00000398832.4:n.-105-4784_-105-4782de...
ENST00000349243.7:c.-47-15593_-47-15591del	ENSP00000273430.3:n.-47-15593_-47-15591de...
ENST00000404754.2:c.-47-15593_-47-15591del	ENSP00000385612.2:n.-47-15593_-47-15591de...
ENST00000475166.5:n.217-4784_217-4782del
ENST00000497524.5:c.-47-15593_-47-15591del	ENSP00000419422.1:n.-47-15593_-47-15591de...
NM_000685.4:c.-47-15593_-47-15591del	NP_000676.1:n.-47-15593_-47-15591del
NM_004835.4:c.1-4784_1-4782del	NP_004826.5:n.1-4784_1-4782del
NM_009585.3:c.-47-15593_-47-15591del	NP_033611.1:n.-47-15593_-47-15591del
NM_031850.3:c.1-4784_1-4782del	NP_114038.4:n.1-4784_1-4782del
NM_000685.5:c.-47-15593_-47-15591del MANE Select	NP_000676.1:n.-47-15593_-47-15591del
NM_001382736.1:c.-47-15593_-47-15591del	NP_001369665.1:n.-47-15593_-47-15591del
NM_001382737.1:c.-47-15593_-47-15591del	NP_001369666.1:n.-47-15593_-47-15591del
NM_004835.5:c.-105-4784_-105-4782del	NP_004826.6:n.-105-4784_-105-4782del
NM_009585.4:c.-47-15593_-47-15591del	NP_033611.1:n.-47-15593_-47-15591del
NM_031850.4:c.-105-4784_-105-4782del	NP_114038.5:n.-105-4784_-105-4782del
NM_032049.4:c.-262-4784_-262-4782del	NP_114438.3:n.-262-4784_-262-4782del