Canonical Allele Identifier: CA2435101945
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67643292C= , CM000685.2:g.67643292C= GRCh38
NC_000023.10:g.66863134C= , CM000685.1:g.66863134C= GRCh37
NC_000023.9:g.66779859C= NCBI36
NG_009014.2:g.104261C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*1C= ENSP00000379358.4:n.*1C=
ENST00000374690.9:c.1653C= MANE Select ENSP00000363822.3:p.Asp551=
ENST00000396043.3:c.280C= ENSP00000379358.3:n.280C=
ENST00000396044.8:c.1653C= ENSP00000379359.3:p.Asp551=
ENST00000612452.5:c.1653C= ENSP00000484033.2:p.Asp551=
ENST00000374690.7:c.1653C= ENSP00000363822.3:p.Asp551=
ENST00000396043.2:c.57C= ENSP00000379358.2:p.Asp19=
ENST00000396044.7:c.1653C= ENSP00000379359.3:p.Asp551=
ENST00000504326.5:c.1653C= ENSP00000421155.1:p.Asp551=
ENST00000513847.5:n.1980C=
ENST00000514029.5:c.1653C= ENSP00000425199.1:p.Asp551=
ENST00000612010.4:c.1653C= ENSP00000482407.1:p.Asp551=
ENST00000612452.4:c.1083C= ENSP00000484033.1:p.Asp361=
ENST00000613054.2:c.1617-42649C= ENSP00000479013.1:n.1617-42649C=
NM_000044.3:c.1653C= NP_000035.2:p.Asp551=
NM_001011645.2:c.57C= NP_001011645.1:p.Asp19=
NM_000044.4:c.1653C= NP_000035.2:p.Asp551=
NM_001011645.3:c.57C= NP_001011645.1:p.Asp19=
NM_001348061.1:c.1653C= NP_001334990.1:p.Asp551=
NM_001348063.1:c.1653C= NP_001334992.1:p.Asp551=
NM_001348064.1:c.1617-42649C= NP_001334993.1:n.1617-42649C=
NM_000044.6:c.1653C= MANE Select NP_000035.2:p.Asp551=