Canonical Allele Identifier: CA413428456

Gene: AR

Linked Data

• ClinVar Variation Id: 2138591
• ClinVar RCV Id: RCV003064730
• dbSNP Id: rs2147540801
• MyVariant Identifiers: chrX:g.66943661C>G (hg19) ; chrX:g.67723819C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723819C>G , CM000685.2:g.67723819C>G	GRCh38
NC_000023.10:g.66943661C>G , CM000685.1:g.66943661C>G	GRCh37
NC_000023.9:g.66860386C>G	NCBI36
NG_009014.2:g.184788C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1089C>G	ENSP00000379358.4:n.*1089C>G
ENST00000374690.9:c.2741C>G MANE Select	ENSP00000363822.3:p.Pro914Arg
ENST00000396043.3:c.1368C>G	ENSP00000379358.3:n.1368C>G
ENST00000396044.8:c.*102C>G	ENSP00000379359.3:n.*102C>G
ENST00000612452.5:c.2741C>G	ENSP00000484033.2:p.Pro914Arg
ENST00000374690.7:c.2741C>G	ENSP00000363822.3:p.Pro914Arg
ENST00000396043.2:c.1145C>G	ENSP00000379358.2:p.Pro382Arg
ENST00000396044.7:c.*102C>G	ENSP00000379359.3:n.*102C>G
ENST00000612452.4:c.2192C>G	ENSP00000484033.1:p.Pro731Arg
NM_000044.3:c.2741C>G	NP_000035.2:p.Pro914Arg
NM_001011645.2:c.1145C>G	NP_001011645.1:p.Pro382Arg
NM_000044.4:c.2741C>G	NP_000035.2:p.Pro914Arg
NM_001011645.3:c.1145C>G	NP_001011645.1:p.Pro382Arg
NM_000044.6:c.2741C>G MANE Select	NP_000035.2:p.Pro914Arg