Canonical Allele Identifier: CA413428008

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942771C>A (hg19) ; chrX:g.67722929C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722929C>A , CM000685.2:g.67722929C>A	GRCh38
NC_000023.10:g.66942771C>A , CM000685.1:g.66942771C>A	GRCh37
NC_000023.9:g.66859496C>A	NCBI36
NG_009014.2:g.183898C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*900C>A	ENSP00000379358.4:n.*900C>A
ENST00000374690.9:c.2552C>A MANE Select	ENSP00000363822.3:p.Thr851Lys
ENST00000396043.3:c.1179C>A	ENSP00000379358.3:n.1179C>A
ENST00000396044.8:c.2174-757C>A	ENSP00000379359.3:n.2174-757C>A
ENST00000612452.5:c.2552C>A	ENSP00000484033.2:p.Thr851Lys
ENST00000374690.7:c.2552C>A	ENSP00000363822.3:p.Thr851Lys
ENST00000396043.2:c.956C>A	ENSP00000379358.2:p.Thr319Lys
ENST00000396044.7:c.2174-757C>A	ENSP00000379359.3:n.2174-757C>A
ENST00000612452.4:c.2003C>A	ENSP00000484033.1:p.Thr668Lys
NM_000044.3:c.2552C>A	NP_000035.2:p.Thr851Lys
NM_001011645.2:c.956C>A	NP_001011645.1:p.Thr319Lys
NM_000044.4:c.2552C>A	NP_000035.2:p.Thr851Lys
NM_001011645.3:c.956C>A	NP_001011645.1:p.Thr319Lys
NM_000044.6:c.2552C>A MANE Select	NP_000035.2:p.Thr851Lys