Canonical Allele Identifier: CA2435101979
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67643395A= , CM000685.2:g.67643395A= GRCh38
NC_000023.10:g.66863237A= , CM000685.1:g.66863237A= GRCh37
NC_000023.9:g.66779962A= NCBI36
NG_009014.2:g.104364A=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*104A= ENSP00000379358.4:n.*104A=
ENST00000374690.9:c.1756A= MANE Select ENSP00000363822.3:p.Arg586=
ENST00000396043.3:c.383A= ENSP00000379358.3:n.383A=
ENST00000396044.8:c.1756A= ENSP00000379359.3:p.Arg586=
ENST00000612452.5:c.1756A= ENSP00000484033.2:p.Arg586=
ENST00000374690.7:c.1756A= ENSP00000363822.3:p.Arg586=
ENST00000396043.2:c.160A= ENSP00000379358.2:p.Arg54=
ENST00000396044.7:c.1756A= ENSP00000379359.3:p.Arg586=
ENST00000504326.5:c.1756A= ENSP00000421155.1:p.Arg586=
ENST00000513847.5:n.2083A=
ENST00000514029.5:c.1756A= ENSP00000425199.1:p.Arg586=
ENST00000612010.4:c.1756A= ENSP00000482407.1:p.Arg586=
ENST00000612452.4:c.1186A= ENSP00000484033.1:p.Arg396=
ENST00000613054.2:c.1617-42546A= ENSP00000479013.1:n.1617-42546A=
NM_000044.3:c.1756A= NP_000035.2:p.Arg586=
NM_001011645.2:c.160A= NP_001011645.1:p.Arg54=
NM_000044.4:c.1756A= NP_000035.2:p.Arg586=
NM_001011645.3:c.160A= NP_001011645.1:p.Arg54=
NM_001348061.1:c.1756A= NP_001334990.1:p.Arg586=
NM_001348063.1:c.1756A= NP_001334992.1:p.Arg586=
NM_001348064.1:c.1617-42546A= NP_001334993.1:n.1617-42546A=
NM_000044.6:c.1756A= MANE Select NP_000035.2:p.Arg586=