Canonical Allele Identifier: CA413427431
Gene: AR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67722827T>C , CM000685.2:g.67722827T>C GRCh38
NC_000023.10:g.66942669T>C , CM000685.1:g.66942669T>C GRCh37
NC_000023.9:g.66859394T>C NCBI36
NG_009014.2:g.183796T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*798T>C ENSP00000379358.4:n.*798T>C
ENST00000374690.9:c.2450T>C MANE Select ENSP00000363822.3:p.Ile817Thr
ENST00000396043.3:c.1077T>C ENSP00000379358.3:n.1077T>C
ENST00000396044.8:c.2174-859T>C ENSP00000379359.3:n.2174-859T>C
ENST00000612452.5:c.2450T>C ENSP00000484033.2:p.Ile817Thr
ENST00000374690.7:c.2450T>C ENSP00000363822.3:p.Ile817Thr
ENST00000396043.2:c.854T>C ENSP00000379358.2:p.Ile285Thr
ENST00000396044.7:c.2174-859T>C ENSP00000379359.3:n.2174-859T>C
ENST00000612452.4:c.1901T>C ENSP00000484033.1:p.Ile634Thr
NM_000044.3:c.2450T>C NP_000035.2:p.Ile817Thr
NM_001011645.2:c.854T>C NP_001011645.1:p.Ile285Thr
NM_000044.4:c.2450T>C NP_000035.2:p.Ile817Thr
NM_001011645.3:c.854T>C NP_001011645.1:p.Ile285Thr
NM_000044.6:c.2450T>C MANE Select NP_000035.2:p.Ile817Thr