Canonical Allele Identifier: CA413428312
Community Standard Title: NM_000044.6(AR):c.2678C>T (p.Pro893Leu)
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723756C>T , CM000685.2:g.67723756C>T GRCh38
NC_000023.10:g.66943598C>T , CM000685.1:g.66943598C>T GRCh37
NC_000023.9:g.66860323C>T NCBI36
NG_009014.2:g.184725C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000044.6:c.2678C>T MANE Select NP_000035.2:p.Pro893Leu
ENST00000374690.9:c.2678C>T MANE Select ENSP00000363822.3:p.Pro893Leu
NM_000044.3:c.2678C>T NP_000035.2:p.Pro893Leu
NM_000044.4:c.2678C>T NP_000035.2:p.Pro893Leu
NM_001011645.2:c.1082C>T NP_001011645.1:p.Pro361Leu
NM_001011645.3:c.1082C>T NP_001011645.1:p.Pro361Leu
ENST00000374690.7:c.2678C>T ENSP00000363822.3:p.Pro893Leu
ENST00000396043.2:c.1082C>T ENSP00000379358.2:p.Pro361Leu
ENST00000396043.3:c.1305C>T ENSP00000379358.3:n.1305C>T
ENST00000396043.4:c.*1026C>T ENSP00000379358.4:n.*1026C>T
ENST00000396044.7:c.*39C>T ENSP00000379359.3:n.*39C>T
ENST00000396044.8:c.*39C>T ENSP00000379359.3:n.*39C>T
ENST00000612452.4:c.2129C>T ENSP00000484033.1:p.Pro710Leu
ENST00000612452.5:c.2678C>T ENSP00000484033.2:p.Pro893Leu