Canonical Allele Identifier: CA120734

Gene: AR

Linked Data

• ClinVar Variation Id: 9830
• ClinVar RCV Id: RCV000010504 ; RCV000010529 ; RCV000640474 ; RCV001269809
• dbSNP Id: rs137852577
• gnomAD v4: X-67722898-C-T
• MyVariant Identifiers: chrX:g.66942740C>T (hg19) ; chrX:g.67722898C>T (hg38)
• PubMed: PMID:8040309 ; PMID:11788673

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722898C>T , CM000685.2:g.67722898C>T	GRCh38
NC_000023.10:g.66942740C>T , CM000685.1:g.66942740C>T	GRCh37
NC_000023.9:g.66859465C>T	NCBI36
NG_009014.2:g.183867C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*869C>T	ENSP00000379358.4:n.*869C>T
ENST00000374690.9:c.2521C>T MANE Select	ENSP00000363822.3:p.Arg841Cys
ENST00000396043.3:c.1148C>T	ENSP00000379358.3:n.1148C>T
ENST00000396044.8:c.2174-788C>T	ENSP00000379359.3:n.2174-788C>T
ENST00000612452.5:c.2521C>T	ENSP00000484033.2:p.Arg841Cys
ENST00000374690.7:c.2521C>T	ENSP00000363822.3:p.Arg841Cys
ENST00000396043.2:c.925C>T	ENSP00000379358.2:p.Arg309Cys
ENST00000396044.7:c.2174-788C>T	ENSP00000379359.3:n.2174-788C>T
ENST00000612452.4:c.1972C>T	ENSP00000484033.1:p.Arg658Cys
NM_000044.3:c.2521C>T	NP_000035.2:p.Arg841Cys
NM_001011645.2:c.925C>T	NP_001011645.1:p.Arg309Cys
NM_000044.4:c.2521C>T	NP_000035.2:p.Arg841Cys
NM_001011645.3:c.925C>T	NP_001011645.1:p.Arg309Cys
NM_000044.6:c.2521C>T MANE Select	NP_000035.2:p.Arg841Cys