Canonical Allele Identifier: CA517048536

Gene: AR

Linked Data

• dbSNP Id: rs2147525106
• MyVariant Identifiers: chrX:g.66931473C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711631C>A , CM000685.2:g.67711631C>A	GRCh38
NC_000023.10:g.66931473C>A , CM000685.1:g.66931473C>A	GRCh37
NC_000023.9:g.66848198C>A	NCBI36
NG_009014.2:g.172600C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*463C>A	ENSP00000379358.4:n.*463C>A
ENST00000374690.9:c.2115C>A MANE Select	ENSP00000363822.3:p.Leu705=
ENST00000396043.3:c.742C>A	ENSP00000379358.3:n.742C>A
ENST00000396044.8:c.2115C>A	ENSP00000379359.3:p.Leu705=
ENST00000612452.5:c.2115C>A	ENSP00000484033.2:p.Leu705=
ENST00000374690.7:c.2115C>A	ENSP00000363822.3:p.Leu705=
ENST00000396043.2:c.519C>A	ENSP00000379358.2:p.Leu173=
ENST00000396044.7:c.2115C>A	ENSP00000379359.3:p.Leu705=
ENST00000612452.4:c.1545C>A	ENSP00000484033.1:p.Leu515=
NM_000044.3:c.2115C>A	NP_000035.2:p.Leu705=
NM_001011645.2:c.519C>A	NP_001011645.1:p.Leu173=
NM_000044.4:c.2115C>A	NP_000035.2:p.Leu705=
NM_001011645.3:c.519C>A	NP_001011645.1:p.Leu173=
NM_000044.6:c.2115C>A MANE Select	NP_000035.2:p.Leu705=