Canonical Allele Identifier: CA2435134336
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721861A= , CM000685.2:g.67721861A= GRCh38
NC_000023.10:g.66941703A= , CM000685.1:g.66941703A= GRCh37
NC_000023.9:g.66858428A= NCBI36
NG_009014.2:g.182830A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*695A= ENSP00000379358.4:n.*695A=
ENST00000374690.9:c.2347A= MANE Select ENSP00000363822.3:p.Ser783=
ENST00000396043.3:c.974A= ENSP00000379358.3:n.974A=
ENST00000396044.8:c.2174-1825A= ENSP00000379359.3:n.2174-1825A=
ENST00000612452.5:c.2347A= ENSP00000484033.2:p.Ser783=
ENST00000374690.7:c.2347A= ENSP00000363822.3:p.Ser783=
ENST00000396043.2:c.751A= ENSP00000379358.2:p.Ser251=
ENST00000396044.7:c.2174-1825A= ENSP00000379359.3:n.2174-1825A=
ENST00000612452.4:c.1777A= ENSP00000484033.1:p.Ser593=
NM_000044.3:c.2347A= NP_000035.2:p.Ser783=
NM_001011645.2:c.751A= NP_001011645.1:p.Ser251=
NM_000044.4:c.2347A= NP_000035.2:p.Ser783=
NM_001011645.3:c.751A= NP_001011645.1:p.Ser251=
NM_000044.6:c.2347A= MANE Select NP_000035.2:p.Ser783=