Canonical Allele Identifier: CA2579630637
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721944_67721948del , CM000685.2:g.67721944_67721948del GRCh38
NC_000023.10:g.66941786_66941790del , CM000685.1:g.66941786_66941790del GRCh37
NC_000023.9:g.66858511_66858515del NCBI36
NG_009014.2:g.182913_182917del

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*778_*782del ENSP00000379358.4:n.*778_*782del
ENST00000374690.9:c.2430_2434del MANE Select ENSP00000363822.3:p.Leu811ThrfsTer17
ENST00000396043.3:c.1057_1061del ENSP00000379358.3:n.1057_1061del
ENST00000396044.8:c.2174-1742_2174-1738del ENSP00000379359.3:n.2174-1742_2174-1738de...
ENST00000612452.5:c.2430_2434del ENSP00000484033.2:p.Leu811ThrfsTer17
ENST00000374690.7:c.2430_2434del ENSP00000363822.3:p.Leu811ThrfsTer17
ENST00000396043.2:c.834_838del ENSP00000379358.2:p.Leu279ThrfsTer17
ENST00000396044.7:c.2174-1742_2174-1738del ENSP00000379359.3:n.2174-1742_2174-1738de...
ENST00000612452.4:c.1860_1864del ENSP00000484033.1:p.Leu621ThrfsTer5
NM_000044.3:c.2430_2434del NP_000035.2:p.Leu811ThrfsTer17
NM_001011645.2:c.834_838del NP_001011645.1:p.Leu279ThrfsTer17
NM_000044.4:c.2430_2434del NP_000035.2:p.Leu811ThrfsTer17
NM_001011645.3:c.834_838del NP_001011645.1:p.Leu279ThrfsTer17
NM_000044.6:c.2430_2434del MANE Select NP_000035.2:p.Leu811ThrfsTer17