Canonical Allele Identifier: CA2435134357
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721937T= , CM000685.2:g.67721937T= GRCh38
NC_000023.10:g.66941779T= , CM000685.1:g.66941779T= GRCh37
NC_000023.9:g.66858504T= NCBI36
NG_009014.2:g.182906T=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*771T= ENSP00000379358.4:n.*771T=
ENST00000374690.9:c.2423T= MANE Select ENSP00000363822.3:p.Met808=
ENST00000396043.3:c.1050T= ENSP00000379358.3:n.1050T=
ENST00000396044.8:c.2174-1749T= ENSP00000379359.3:n.2174-1749T=
ENST00000612452.5:c.2423T= ENSP00000484033.2:p.Met808=
ENST00000374690.7:c.2423T= ENSP00000363822.3:p.Met808=
ENST00000396043.2:c.827T= ENSP00000379358.2:p.Met276=
ENST00000396044.7:c.2174-1749T= ENSP00000379359.3:n.2174-1749T=
ENST00000612452.4:c.1853T= ENSP00000484033.1:p.Met618=
NM_000044.3:c.2423T= NP_000035.2:p.Met808=
NM_001011645.2:c.827T= NP_001011645.1:p.Met276=
NM_000044.4:c.2423T= NP_000035.2:p.Met808=
NM_001011645.3:c.827T= NP_001011645.1:p.Met276=
NM_000044.6:c.2423T= MANE Select NP_000035.2:p.Met808=