Canonical Allele Identifier: CA2821592992
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67544862_67544865del , CM000685.2:g.67544862_67544865del GRCh38
NC_000023.10:g.66764704_66764707del , CM000685.1:g.66764704_66764707del GRCh37
NC_000023.9:g.66681429_66681432del NCBI36
NG_009014.2:g.5831_5834del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.-285_-282del ENSP00000379358.4:n.-285_-282del
ENST00000374690.9:c.-285_-282del MANE Select ENSP00000363822.3:n.-285_-282del
ENST00000612452.5:c.-285_-282del ENSP00000484033.2:n.-285_-282del
ENST00000374690.7:c.-285_-282del ENSP00000363822.3:n.-285_-282del
ENST00000396044.7:c.-285_-282del ENSP00000379359.3:n.-285_-282del
ENST00000504326.5:c.-285_-282del ENSP00000421155.1:n.-285_-282del
ENST00000513847.5:n.43_46del
ENST00000514029.5:c.-285_-282del ENSP00000425199.1:n.-285_-282del
ENST00000612010.4:c.-285_-282del ENSP00000482407.1:n.-285_-282del
ENST00000612452.4:c.-855_-852del ENSP00000484033.1:n.-855_-852del
ENST00000613054.2:c.-285_-282del ENSP00000479013.1:n.-285_-282del
NM_000044.3:c.-285_-282del NP_000035.2:n.-285_-282del
NM_000044.4:c.-285_-282del NP_000035.2:n.-285_-282del
NM_001011645.3:c.-2068_-2065del NP_001011645.1:n.-2068_-2065del
NM_001348061.1:c.-285_-282del NP_001334990.1:n.-285_-282del
NM_001348063.1:c.-285_-282del NP_001334992.1:n.-285_-282del
NM_001348064.1:c.-285_-282del NP_001334993.1:n.-285_-282del
NM_000044.6:c.-285_-282del MANE Select NP_000035.2:n.-285_-282del