Canonical Allele Identifier: CA413429305

Gene: AR

Linked Data

• ClinVar Variation Id: 434266
• ClinVar RCV Id: RCV000499725
• dbSNP Id: rs1555990485
• COSMIC: COSM1124203 ; COSM1124204
• MyVariant Identifiers: chrX:g.66905929C>T (hg19) ; chrX:g.67686087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686087C>T , CM000685.2:g.67686087C>T	GRCh38
NC_000023.10:g.66905929C>T , CM000685.1:g.66905929C>T	GRCh37
NC_000023.9:g.66822654C>T	NCBI36
NG_009014.2:g.147056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*194C>T	ENSP00000379358.4:n.*194C>T
ENST00000374690.9:c.1846C>T MANE Select	ENSP00000363822.3:p.Arg616Cys
ENST00000396043.3:c.473C>T	ENSP00000379358.3:n.473C>T
ENST00000396044.8:c.1846C>T	ENSP00000379359.3:p.Arg616Cys
ENST00000612452.5:c.1846C>T	ENSP00000484033.2:p.Arg616Cys
ENST00000374690.7:c.1846C>T	ENSP00000363822.3:p.Arg616Cys
ENST00000396043.2:c.250C>T	ENSP00000379358.2:p.Arg84Cys
ENST00000396044.7:c.1846C>T	ENSP00000379359.3:p.Arg616Cys
ENST00000504326.5:c.1846C>T	ENSP00000421155.1:p.Arg616Cys
ENST00000513847.5:n.2173C>T
ENST00000514029.5:c.*327C>T	ENSP00000425199.1:n.*327C>T
ENST00000612010.4:c.*198C>T	ENSP00000482407.1:n.*198C>T
ENST00000612452.4:c.1276C>T	ENSP00000484033.1:p.Arg426Cys
ENST00000613054.2:c.*44C>T	ENSP00000479013.1:n.*44C>T
NM_000044.3:c.1846C>T	NP_000035.2:p.Arg616Cys
NM_001011645.2:c.250C>T	NP_001011645.1:p.Arg84Cys
NM_000044.4:c.1846C>T	NP_000035.2:p.Arg616Cys
NM_001011645.3:c.250C>T	NP_001011645.1:p.Arg84Cys
NM_001348061.1:c.1846C>T	NP_001334990.1:p.Arg616Cys
NM_001348063.1:c.1846C>T	NP_001334992.1:p.Arg616Cys
NM_001348064.1:c.*44C>T	NP_001334993.1:n.*44C>T
NM_000044.6:c.1846C>T MANE Select	NP_000035.2:p.Arg616Cys