Canonical Allele Identifier: CA413428260

Gene: AR

Linked Data

• dbSNP Id: rs2076147009
• gnomAD v4: X-67723736-C-A
• MyVariant Identifiers: chrX:g.66943578C>A (hg19) ; chrX:g.67723736C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723736C>A , CM000685.2:g.67723736C>A	GRCh38
NC_000023.10:g.66943578C>A , CM000685.1:g.66943578C>A	GRCh37
NC_000023.9:g.66860303C>A	NCBI36
NG_009014.2:g.184705C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1006C>A	ENSP00000379358.4:n.*1006C>A
ENST00000374690.9:c.2658C>A MANE Select	ENSP00000363822.3:p.His886Gln
ENST00000396043.3:c.1285C>A	ENSP00000379358.3:n.1285C>A
ENST00000396044.8:c.*19C>A	ENSP00000379359.3:n.*19C>A
ENST00000612452.5:c.2658C>A	ENSP00000484033.2:p.His886Gln
ENST00000374690.7:c.2658C>A	ENSP00000363822.3:p.His886Gln
ENST00000396043.2:c.1062C>A	ENSP00000379358.2:p.His354Gln
ENST00000396044.7:c.*19C>A	ENSP00000379359.3:n.*19C>A
ENST00000612452.4:c.2109C>A	ENSP00000484033.1:p.His703Gln
NM_000044.3:c.2658C>A	NP_000035.2:p.His886Gln
NM_001011645.2:c.1062C>A	NP_001011645.1:p.His354Gln
NM_000044.4:c.2658C>A	NP_000035.2:p.His886Gln
NM_001011645.3:c.1062C>A	NP_001011645.1:p.His354Gln
NM_000044.6:c.2658C>A MANE Select	NP_000035.2:p.His886Gln