Canonical Allele Identifier: CA2657435

Gene: AGTR1

Linked Data

• dbSNP Id: rs753563079
• ExAC: 3:148459864 TCCA / T
• gnomAD v2: 3-148459864-TCCA-T
• gnomAD v3: 3-148742077-TCCA-T
• gnomAD v4: 3-148742077-TCCA-T
• MyVariant Identifiers: chr3:g.148459865_148459867del (hg19) ; chr3:g.148742078_148742080del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742081_148742083del , CM000665.2:g.148742081_148742083del	GRCh38
NC_000003.11:g.148459868_148459870del , CM000665.1:g.148459868_148459870del	GRCh37
NC_000003.10:g.149942558_149942560del	NCBI36
NG_008468.1:g.49211_49213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.1046_1048del MANE Select	ENSP00000273430.3:p.Thr349del
ENST00000402260.2:c.1046_1048del	ENSP00000385641.3:p.Thr349del
ENST00000418473.7:c.1046_1048del	ENSP00000398832.4:p.Thr349del
ENST00000349243.7:c.1046_1048del	ENSP00000273430.3:p.Thr349del
ENST00000402260.1:c.1133_1135del	ENSP00000385641.2:p.Thr378del
ENST00000404754.2:c.1046_1048del	ENSP00000385612.2:p.Thr349del
ENST00000418473.6:c.1151_1153del	ENSP00000398832.3:p.Thr384del
ENST00000461609.1:c.1046_1048del	ENSP00000418851.1:p.Thr349del
ENST00000474935.5:c.1046_1048del	ENSP00000418084.1:p.Thr349del
ENST00000475347.5:c.1046_1048del	ENSP00000419783.1:p.Thr349del
ENST00000497524.5:c.1046_1048del	ENSP00000419422.1:p.Thr349del
NM_000685.4:c.1046_1048del	NP_000676.1:p.Thr349del
NM_004835.4:c.1151_1153del	NP_004826.5:p.Thr384del
NM_009585.3:c.1046_1048del	NP_033611.1:p.Thr349del
NM_031850.3:c.1151_1153del	NP_114038.4:p.Thr384del
NM_032049.3:c.1133_1135del	NP_114438.2:p.Thr378del
NM_000685.5:c.1046_1048del MANE Select	NP_000676.1:p.Thr349del
NM_001382736.1:c.1046_1048del	NP_001369665.1:p.Thr349del
NM_001382737.1:c.1046_1048del	NP_001369666.1:p.Thr349del
NM_004835.5:c.1046_1048del	NP_004826.6:p.Thr349del
NM_009585.4:c.1046_1048del	NP_033611.1:p.Thr349del
NM_031850.4:c.1046_1048del	NP_114038.5:p.Thr349del
NM_032049.4:c.1046_1048del	NP_114438.3:p.Thr349del