Canonical Allele Identifier: CA413423392

Gene: AR

Linked Data

• ClinVar Variation Id: 434267
• ClinVar RCV Id: RCV000501357
• dbSNP Id: rs1555995842
• MyVariant Identifiers: chrX:g.66931448C>A (hg19) ; chrX:g.67711606C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711606C>A , CM000685.2:g.67711606C>A	GRCh38
NC_000023.10:g.66931448C>A , CM000685.1:g.66931448C>A	GRCh37
NC_000023.9:g.66848173C>A	NCBI36
NG_009014.2:g.172575C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*438C>A	ENSP00000379358.4:n.*438C>A
ENST00000374690.9:c.2090C>A MANE Select	ENSP00000363822.3:p.Ser697Tyr
ENST00000396043.3:c.717C>A	ENSP00000379358.3:n.717C>A
ENST00000396044.8:c.2090C>A	ENSP00000379359.3:p.Ser697Tyr
ENST00000612452.5:c.2090C>A	ENSP00000484033.2:p.Ser697Tyr
ENST00000374690.7:c.2090C>A	ENSP00000363822.3:p.Ser697Tyr
ENST00000396043.2:c.494C>A	ENSP00000379358.2:p.Ser165Tyr
ENST00000396044.7:c.2090C>A	ENSP00000379359.3:p.Ser697Tyr
ENST00000612452.4:c.1520C>A	ENSP00000484033.1:p.Ser507Tyr
NM_000044.3:c.2090C>A	NP_000035.2:p.Ser697Tyr
NM_001011645.2:c.494C>A	NP_001011645.1:p.Ser165Tyr
NM_000044.4:c.2090C>A	NP_000035.2:p.Ser697Tyr
NM_001011645.3:c.494C>A	NP_001011645.1:p.Ser165Tyr
NM_000044.6:c.2090C>A MANE Select	NP_000035.2:p.Ser697Tyr