Canonical Allele Identifier: CA413424520
Community Standard Title: NM_000044.6(AR):c.2225G>T (p.Trp742Leu)
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717529G>T , CM000685.2:g.67717529G>T GRCh38
NC_000023.10:g.66937371G>T , CM000685.1:g.66937371G>T GRCh37
NC_000023.9:g.66854096G>T NCBI36
NG_009014.2:g.178498G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000044.6:c.2225G>T MANE Select NP_000035.2:p.Trp742Leu
ENST00000374690.9:c.2225G>T MANE Select ENSP00000363822.3:p.Trp742Leu
NM_000044.3:c.2225G>T NP_000035.2:p.Trp742Leu
NM_000044.4:c.2225G>T NP_000035.2:p.Trp742Leu
NM_001011645.2:c.629G>T NP_001011645.1:p.Trp210Leu
NM_001011645.3:c.629G>T NP_001011645.1:p.Trp210Leu
ENST00000374690.7:c.2225G>T ENSP00000363822.3:p.Trp742Leu
ENST00000396043.2:c.629G>T ENSP00000379358.2:p.Trp210Leu
ENST00000396043.3:c.852G>T ENSP00000379358.3:n.852G>T
ENST00000396043.4:c.*573G>T ENSP00000379358.4:n.*573G>T
ENST00000396044.7:c.2173+5840G>T ENSP00000379359.3:n.2173+5840G>T
ENST00000396044.8:c.2173+5840G>T ENSP00000379359.3:n.2173+5840G>T
ENST00000612452.4:c.1655G>T ENSP00000484033.1:p.Trp552Leu
ENST00000612452.5:c.2225G>T ENSP00000484033.2:p.Trp742Leu