Canonical Allele Identifier: CA413429329
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 854942
ClinVar RCV Id: RCV001060093
dbSNP Id: rs1312745277

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67686100G>A , CM000685.2:g.67686100G>A GRCh38
NC_000023.10:g.66905942G>A , CM000685.1:g.66905942G>A GRCh37
NC_000023.9:g.66822667G>A NCBI36
NG_009014.2:g.147069G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*207G>A ENSP00000379358.4:n.*207G>A
ENST00000374690.9:c.1859G>A MANE Select ENSP00000363822.3:p.Cys620Tyr
ENST00000396043.3:c.486G>A ENSP00000379358.3:n.486G>A
ENST00000396044.8:c.1859G>A ENSP00000379359.3:p.Cys620Tyr
ENST00000612452.5:c.1859G>A ENSP00000484033.2:p.Cys620Tyr
ENST00000374690.7:c.1859G>A ENSP00000363822.3:p.Cys620Tyr
ENST00000396043.2:c.263G>A ENSP00000379358.2:p.Cys88Tyr
ENST00000396044.7:c.1859G>A ENSP00000379359.3:p.Cys620Tyr
ENST00000504326.5:c.1859G>A ENSP00000421155.1:p.Cys620Tyr
ENST00000513847.5:n.2186G>A
ENST00000514029.5:c.*340G>A ENSP00000425199.1:n.*340G>A
ENST00000612010.4:c.*211G>A ENSP00000482407.1:n.*211G>A
ENST00000612452.4:c.1289G>A ENSP00000484033.1:p.Cys430Tyr
ENST00000613054.2:c.*57G>A ENSP00000479013.1:n.*57G>A
NM_000044.3:c.1859G>A NP_000035.2:p.Cys620Tyr
NM_001011645.2:c.263G>A NP_001011645.1:p.Cys88Tyr
NM_000044.4:c.1859G>A NP_000035.2:p.Cys620Tyr
NM_001011645.3:c.263G>A NP_001011645.1:p.Cys88Tyr
NM_001348061.1:c.1859G>A NP_001334990.1:p.Cys620Tyr
NM_001348063.1:c.1859G>A NP_001334992.1:p.Cys620Tyr
NM_001348064.1:c.*57G>A NP_001334993.1:n.*57G>A
NM_000044.6:c.1859G>A MANE Select NP_000035.2:p.Cys620Tyr