Canonical Allele Identifier: CA413428089
Community Standard Title: NM_000044.6(AR):c.2591T>C (p.Leu864Pro)
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67722968T>C , CM000685.2:g.67722968T>C GRCh38
NC_000023.10:g.66942810T>C , CM000685.1:g.66942810T>C GRCh37
NC_000023.9:g.66859535T>C NCBI36
NG_009014.2:g.183937T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000044.6:c.2591T>C MANE Select NP_000035.2:p.Leu864Pro
ENST00000374690.9:c.2591T>C MANE Select ENSP00000363822.3:p.Leu864Pro
NM_000044.3:c.2591T>C NP_000035.2:p.Leu864Pro
NM_000044.4:c.2591T>C NP_000035.2:p.Leu864Pro
NM_001011645.2:c.995T>C NP_001011645.1:p.Leu332Pro
NM_001011645.3:c.995T>C NP_001011645.1:p.Leu332Pro
ENST00000374690.7:c.2591T>C ENSP00000363822.3:p.Leu864Pro
ENST00000396043.2:c.995T>C ENSP00000379358.2:p.Leu332Pro
ENST00000396043.3:c.1218T>C ENSP00000379358.3:n.1218T>C
ENST00000396043.4:c.*939T>C ENSP00000379358.4:n.*939T>C
ENST00000396044.7:c.2174-718T>C ENSP00000379359.3:n.2174-718T>C
ENST00000396044.8:c.2174-718T>C ENSP00000379359.3:n.2174-718T>C
ENST00000612452.4:c.2042T>C ENSP00000484033.1:p.Leu681Pro
ENST00000612452.5:c.2591T>C ENSP00000484033.2:p.Leu864Pro