Canonical Allele Identifier: CA2435132663
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67717599C= , CM000685.2:g.67717599C= GRCh38
NC_000023.10:g.66937441C= , CM000685.1:g.66937441C= GRCh37
NC_000023.9:g.66854166C= NCBI36
NG_009014.2:g.178568C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*643C= ENSP00000379358.4:n.*643C=
ENST00000374690.9:c.2295C= MANE Select ENSP00000363822.3:p.Phe765=
ENST00000396043.3:c.922C= ENSP00000379358.3:n.922C=
ENST00000396044.8:c.2173+5910C= ENSP00000379359.3:n.2173+5910C=
ENST00000612452.5:c.2295C= ENSP00000484033.2:p.Phe765=
ENST00000374690.7:c.2295C= ENSP00000363822.3:p.Phe765=
ENST00000396043.2:c.699C= ENSP00000379358.2:p.Phe233=
ENST00000396044.7:c.2173+5910C= ENSP00000379359.3:n.2173+5910C=
ENST00000612452.4:c.1725C= ENSP00000484033.1:p.Phe575=
NM_000044.3:c.2295C= NP_000035.2:p.Phe765=
NM_001011645.2:c.699C= NP_001011645.1:p.Phe233=
NM_000044.4:c.2295C= NP_000035.2:p.Phe765=
NM_001011645.3:c.699C= NP_001011645.1:p.Phe233=
NM_000044.6:c.2295C= MANE Select NP_000035.2:p.Phe765=