Canonical Allele Identifier: CA120715

Gene: AR

Linked Data

• ClinVar Variation Id: 9820
• ClinVar RCV Id: RCV000010494 ; RCV000382955 ; RCV000806067
• dbSNP Id: rs137852573
• COSMIC: COSM4836194 ; COSM4836195 ; COSM5726996
• MyVariant Identifiers: chrX:g.66905906G>A (hg19) ; chrX:g.67686064G>A (hg38)
• PubMed: PMID:1303262 ; PMID:9543136

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686064G>A , CM000685.2:g.67686064G>A	GRCh38
NC_000023.10:g.66905906G>A , CM000685.1:g.66905906G>A	GRCh37
NC_000023.9:g.66822631G>A	NCBI36
NG_009014.2:g.147033G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*171G>A	ENSP00000379358.4:n.*171G>A
ENST00000374690.9:c.1823G>A MANE Select	ENSP00000363822.3:p.Arg608Gln
ENST00000396043.3:c.450G>A	ENSP00000379358.3:n.450G>A
ENST00000396044.8:c.1823G>A	ENSP00000379359.3:p.Arg608Gln
ENST00000612452.5:c.1823G>A	ENSP00000484033.2:p.Arg608Gln
ENST00000374690.7:c.1823G>A	ENSP00000363822.3:p.Arg608Gln
ENST00000396043.2:c.227G>A	ENSP00000379358.2:p.Arg76Gln
ENST00000396044.7:c.1823G>A	ENSP00000379359.3:p.Arg608Gln
ENST00000504326.5:c.1823G>A	ENSP00000421155.1:p.Arg608Gln
ENST00000513847.5:n.2150G>A
ENST00000514029.5:c.*304G>A	ENSP00000425199.1:n.*304G>A
ENST00000612010.4:c.*175G>A	ENSP00000482407.1:n.*175G>A
ENST00000612452.4:c.1253G>A	ENSP00000484033.1:p.Arg418Gln
ENST00000613054.2:c.*21G>A	ENSP00000479013.1:n.*21G>A
NM_000044.3:c.1823G>A	NP_000035.2:p.Arg608Gln
NM_001011645.2:c.227G>A	NP_001011645.1:p.Arg76Gln
NM_000044.4:c.1823G>A	NP_000035.2:p.Arg608Gln
NM_001011645.3:c.227G>A	NP_001011645.1:p.Arg76Gln
NM_001348061.1:c.1823G>A	NP_001334990.1:p.Arg608Gln
NM_001348063.1:c.1823G>A	NP_001334992.1:p.Arg608Gln
NM_001348064.1:c.*21G>A	NP_001334993.1:n.*21G>A
NM_000044.6:c.1823G>A MANE Select	NP_000035.2:p.Arg608Gln