Canonical Allele Identifier: CA413424759

Gene: AR

Linked Data

• ClinVar Variation Id: 458363
• ClinVar RCV Id: RCV001270001
• dbSNP Id: rs1555996863
• gnomAD v3: X-67717600-G-A
• gnomAD v4: X-67717600-G-A
• MyVariant Identifiers: chrX:g.66937442G>A (hg19) ; chrX:g.67717600G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717600G>A , CM000685.2:g.67717600G>A	GRCh38
NC_000023.10:g.66937442G>A , CM000685.1:g.66937442G>A	GRCh37
NC_000023.9:g.66854167G>A	NCBI36
NG_009014.2:g.178569G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*644G>A	ENSP00000379358.4:n.*644G>A
ENST00000374690.9:c.2296G>A MANE Select	ENSP00000363822.3:p.Ala766Thr
ENST00000396043.3:c.923G>A	ENSP00000379358.3:n.923G>A
ENST00000396044.8:c.2173+5911G>A	ENSP00000379359.3:n.2173+5911G>A
ENST00000612452.5:c.2296G>A	ENSP00000484033.2:p.Ala766Thr
ENST00000374690.7:c.2296G>A	ENSP00000363822.3:p.Ala766Thr
ENST00000396043.2:c.700G>A	ENSP00000379358.2:p.Ala234Thr
ENST00000396044.7:c.2173+5911G>A	ENSP00000379359.3:n.2173+5911G>A
ENST00000612452.4:c.1726G>A	ENSP00000484033.1:p.Ala576Thr
NM_000044.3:c.2296G>A	NP_000035.2:p.Ala766Thr
NM_001011645.2:c.700G>A	NP_001011645.1:p.Ala234Thr
NM_000044.4:c.2296G>A	NP_000035.2:p.Ala766Thr
NM_001011645.3:c.700G>A	NP_001011645.1:p.Ala234Thr
NM_000044.6:c.2296G>A MANE Select	NP_000035.2:p.Ala766Thr