Canonical Allele Identifier: CA413428264

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66943580T>A (hg19) ; chrX:g.67723738T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723738T>A , CM000685.2:g.67723738T>A	GRCh38
NC_000023.10:g.66943580T>A , CM000685.1:g.66943580T>A	GRCh37
NC_000023.9:g.66860305T>A	NCBI36
NG_009014.2:g.184707T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1008T>A	ENSP00000379358.4:n.*1008T>A
ENST00000374690.9:c.2660T>A MANE Select	ENSP00000363822.3:p.Met887Lys
ENST00000396043.3:c.1287T>A	ENSP00000379358.3:n.1287T>A
ENST00000396044.8:c.*21T>A	ENSP00000379359.3:n.*21T>A
ENST00000612452.5:c.2660T>A	ENSP00000484033.2:p.Met887Lys
ENST00000374690.7:c.2660T>A	ENSP00000363822.3:p.Met887Lys
ENST00000396043.2:c.1064T>A	ENSP00000379358.2:p.Met355Lys
ENST00000396044.7:c.*21T>A	ENSP00000379359.3:n.*21T>A
ENST00000612452.4:c.2111T>A	ENSP00000484033.1:p.Met704Lys
NM_000044.3:c.2660T>A	NP_000035.2:p.Met887Lys
NM_001011645.2:c.1064T>A	NP_001011645.1:p.Met355Lys
NM_000044.4:c.2660T>A	NP_000035.2:p.Met887Lys
NM_001011645.3:c.1064T>A	NP_001011645.1:p.Met355Lys
NM_000044.6:c.2660T>A MANE Select	NP_000035.2:p.Met887Lys