Canonical Allele Identifier: CA2435065980
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67544849_67544850delinsGT , CM000685.2:g.67544849_67544850delinsGT GRCh38
NC_000023.10:g.66764691_66764692delinsGT , CM000685.1:g.66764691_66764692delinsGT GRCh37
NC_000023.9:g.66681416_66681417delinsGT NCBI36
NG_009014.2:g.5818_5819delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.-298_-297delinsGT ENSP00000379358.4:n.-298_-297delinsGT
ENST00000374690.9:c.-298_-297delinsGT MANE Select ENSP00000363822.3:n.-298_-297delinsGT
ENST00000612452.5:c.-298_-297delinsGT ENSP00000484033.2:n.-298_-297delinsGT
ENST00000374690.7:c.-298_-297delinsGT ENSP00000363822.3:n.-298_-297delinsGT
ENST00000396044.7:c.-298_-297delinsGT ENSP00000379359.3:n.-298_-297delinsGT
ENST00000504326.5:c.-298_-297delinsGT ENSP00000421155.1:n.-298_-297delinsGT
ENST00000513847.5:n.30_31delinsGT
ENST00000514029.5:c.-298_-297delinsGT ENSP00000425199.1:n.-298_-297delinsGT
ENST00000612010.4:c.-298_-297delinsGT ENSP00000482407.1:n.-298_-297delinsGT
ENST00000612452.4:c.-868_-867delinsGT ENSP00000484033.1:n.-868_-867delinsGT
ENST00000613054.2:c.-298_-297delinsGT ENSP00000479013.1:n.-298_-297delinsGT
NM_000044.3:c.-298_-297delinsGT NP_000035.2:n.-298_-297delinsGT
NM_000044.4:c.-298_-297delinsGT NP_000035.2:n.-298_-297delinsGT
NM_001011645.3:c.-2081_-2080delinsGT NP_001011645.1:n.-2081_-2080delinsGT
NM_001348061.1:c.-298_-297delinsGT NP_001334990.1:n.-298_-297delinsGT
NM_001348063.1:c.-298_-297delinsGT NP_001334992.1:n.-298_-297delinsGT
NM_001348064.1:c.-298_-297delinsGT NP_001334993.1:n.-298_-297delinsGT
NM_000044.6:c.-298_-297delinsGT MANE Select NP_000035.2:n.-298_-297delinsGT