Canonical Allele Identifier: CA1409904256
Gene: AGTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148719960_148719961delinsAT , CM000665.2:g.148719960_148719961delinsAT GRCh38
NC_000003.11:g.148437747_148437748delinsAT , CM000665.1:g.148437747_148437748delinsAT GRCh37
NC_000003.10:g.149920437_149920438delinsAT NCBI36
NG_008468.1:g.27090_27091delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-48+11933_-48+11934delinsAT MANE Select ENSP00000273430.3:n.-48+11933_-48+11934de...
ENST00000418473.7:c.-105-10220_-105-10219delinsAT ENSP00000398832.4:n.-105-10220_-105-10219...
ENST00000349243.7:c.-48+11933_-48+11934delinsAT ENSP00000273430.3:n.-48+11933_-48+11934de...
ENST00000404754.2:c.-47-21029_-47-21028delinsAT ENSP00000385612.2:n.-47-21029_-47-21028de...
ENST00000475166.5:n.217-10220_217-10219delinsAT
ENST00000497524.5:c.-47-21029_-47-21028delinsAT ENSP00000419422.1:n.-47-21029_-47-21028de...
NM_000685.4:c.-48+11933_-48+11934delinsAT NP_000676.1:n.-48+11933_-48+11934delinsAT...
NM_004835.4:c.1-10220_1-10219delinsAT NP_004826.5:n.1-10220_1-10219delinsAT
NM_009585.3:c.-47-21029_-47-21028delinsAT NP_033611.1:n.-47-21029_-47-21028delinsAT...
NM_031850.3:c.1-10220_1-10219delinsAT NP_114038.4:n.1-10220_1-10219delinsAT
NM_000685.5:c.-48+11933_-48+11934delinsAT MANE Select NP_000676.1:n.-48+11933_-48+11934delinsAT...
NM_001382736.1:c.-47-21029_-47-21028delinsAT NP_001369665.1:n.-47-21029_-47-21028delin...
NM_001382737.1:c.-48+11933_-48+11934delinsAT NP_001369666.1:n.-48+11933_-48+11934delin...
NM_004835.5:c.-105-10220_-105-10219delinsAT NP_004826.6:n.-105-10220_-105-10219delins...
NM_009585.4:c.-47-21029_-47-21028delinsAT NP_033611.1:n.-47-21029_-47-21028delinsAT...
NM_031850.4:c.-105-10220_-105-10219delinsAT NP_114038.5:n.-105-10220_-105-10219delins...
NM_032049.4:c.-262-10220_-262-10219delinsAT NP_114438.3:n.-262-10220_-262-10219delins...