Canonical Allele Identifier: CA16621465

Gene: AR

Linked Data

• ClinVar Variation Id: 419720
• ClinVar RCV Id: RCV000481893
• dbSNP Id: rs1064794065
• MyVariant Identifiers: chrX:g.66937443C>A (hg19) ; chrX:g.67717601C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717601C>A , CM000685.2:g.67717601C>A	GRCh38
NC_000023.10:g.66937443C>A , CM000685.1:g.66937443C>A	GRCh37
NC_000023.9:g.66854168C>A	NCBI36
NG_009014.2:g.178570C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*645C>A	ENSP00000379358.4:n.*645C>A
ENST00000374690.9:c.2297C>A MANE Select	ENSP00000363822.3:p.Ala766Asp
ENST00000396043.3:c.924C>A	ENSP00000379358.3:n.924C>A
ENST00000396044.8:c.2173+5912C>A	ENSP00000379359.3:n.2173+5912C>A
ENST00000612452.5:c.2297C>A	ENSP00000484033.2:p.Ala766Asp
ENST00000374690.7:c.2297C>A	ENSP00000363822.3:p.Ala766Asp
ENST00000396043.2:c.701C>A	ENSP00000379358.2:p.Ala234Asp
ENST00000396044.7:c.2173+5912C>A	ENSP00000379359.3:n.2173+5912C>A
ENST00000612452.4:c.1727C>A	ENSP00000484033.1:p.Ala576Asp
NM_000044.3:c.2297C>A	NP_000035.2:p.Ala766Asp
NM_001011645.2:c.701C>A	NP_001011645.1:p.Ala234Asp
NM_000044.4:c.2297C>A	NP_000035.2:p.Ala766Asp
NM_001011645.3:c.701C>A	NP_001011645.1:p.Ala234Asp
NM_000044.6:c.2297C>A MANE Select	NP_000035.2:p.Ala766Asp