Canonical Allele Identifier: CA413423565
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs2147525357
COSMIC: COSM93905

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67711686C>A , CM000685.2:g.67711686C>A GRCh38
NC_000023.10:g.66931528C>A , CM000685.1:g.66931528C>A GRCh37
NC_000023.9:g.66848253C>A NCBI36
NG_009014.2:g.172655C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*518C>A ENSP00000379358.4:n.*518C>A
ENST00000374690.9:c.2170C>A MANE Select ENSP00000363822.3:p.Pro724Thr
ENST00000396043.3:c.797C>A ENSP00000379358.3:n.797C>A
ENST00000396044.8:c.2170C>A ENSP00000379359.3:p.Pro724Thr
ENST00000612452.5:c.2170C>A ENSP00000484033.2:p.Pro724Thr
ENST00000374690.7:c.2170C>A ENSP00000363822.3:p.Pro724Thr
ENST00000396043.2:c.574C>A ENSP00000379358.2:p.Pro192Thr
ENST00000396044.7:c.2170C>A ENSP00000379359.3:p.Pro724Thr
ENST00000612452.4:c.1600C>A ENSP00000484033.1:p.Pro534Thr
NM_000044.3:c.2170C>A NP_000035.2:p.Pro724Thr
NM_001011645.2:c.574C>A NP_001011645.1:p.Pro192Thr
NM_000044.4:c.2170C>A NP_000035.2:p.Pro724Thr
NM_001011645.3:c.574C>A NP_001011645.1:p.Pro192Thr
NM_000044.6:c.2170C>A MANE Select NP_000035.2:p.Pro724Thr