Canonical Allele Identifier: CA2693950198
Gene: AR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717420_67717425del , CM000685.2:g.67717420_67717425del GRCh38
NC_000023.10:g.66937262_66937267del , CM000685.1:g.66937262_66937267del GRCh37
NC_000023.9:g.66853987_66853992del NCBI36
NG_009014.2:g.178389_178394del

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*522-58_*522-53del ENSP00000379358.4:n.*522-58_*522-53del
ENST00000374690.9:c.2174-58_2174-53del MANE Select ENSP00000363822.3:n.2174-58_2174-53del
ENST00000396043.3:c.801-58_801-53del ENSP00000379358.3:n.801-58_801-53del
ENST00000396044.8:c.2173+5731_2173+5736del ENSP00000379359.3:n.2173+5731_2173+5736del
ENST00000612452.5:c.2174-58_2174-53del ENSP00000484033.2:n.2174-58_2174-53del
ENST00000374690.7:c.2174-58_2174-53del ENSP00000363822.3:n.2174-58_2174-53del
ENST00000396043.2:c.578-58_578-53del ENSP00000379358.2:n.578-58_578-53del
ENST00000396044.7:c.2173+5731_2173+5736del ENSP00000379359.3:n.2173+5731_2173+5736del
ENST00000612452.4:c.1604-58_1604-53del ENSP00000484033.1:n.1604-58_1604-53del
NM_000044.3:c.2174-58_2174-53del NP_000035.2:n.2174-58_2174-53del
NM_001011645.2:c.578-58_578-53del NP_001011645.1:n.578-58_578-53del
NM_000044.4:c.2174-58_2174-53del NP_000035.2:n.2174-58_2174-53del
NM_001011645.3:c.578-58_578-53del NP_001011645.1:n.578-58_578-53del
NM_000044.6:c.2174-58_2174-53del MANE Select NP_000035.2:n.2174-58_2174-53del