Canonical Allele Identifier: CA413423537

Gene: AR

Linked Data

• ClinVar Variation Id: 2138586
• ClinVar RCV Id: RCV003064729
• dbSNP Id: rs2147525286
• MyVariant Identifiers: chrX:g.66931514G>A (hg19) ; chrX:g.67711672G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711672G>A , CM000685.2:g.67711672G>A	GRCh38
NC_000023.10:g.66931514G>A , CM000685.1:g.66931514G>A	GRCh37
NC_000023.9:g.66848239G>A	NCBI36
NG_009014.2:g.172641G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*504G>A	ENSP00000379358.4:n.*504G>A
ENST00000374690.9:c.2156G>A MANE Select	ENSP00000363822.3:p.Trp719Ter
ENST00000396043.3:c.783G>A	ENSP00000379358.3:n.783G>A
ENST00000396044.8:c.2156G>A	ENSP00000379359.3:p.Trp719Ter
ENST00000612452.5:c.2156G>A	ENSP00000484033.2:p.Trp719Ter
ENST00000374690.7:c.2156G>A	ENSP00000363822.3:p.Trp719Ter
ENST00000396043.2:c.560G>A	ENSP00000379358.2:p.Trp187Ter
ENST00000396044.7:c.2156G>A	ENSP00000379359.3:p.Trp719Ter
ENST00000612452.4:c.1586G>A	ENSP00000484033.1:p.Trp529Ter
NM_000044.3:c.2156G>A	NP_000035.2:p.Trp719Ter
NM_001011645.2:c.560G>A	NP_001011645.1:p.Trp187Ter
NM_000044.4:c.2156G>A	NP_000035.2:p.Trp719Ter
NM_001011645.3:c.560G>A	NP_001011645.1:p.Trp187Ter
NM_000044.6:c.2156G>A MANE Select	NP_000035.2:p.Trp719Ter