Canonical Allele Identifier: CA413427998

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942766T>A (hg19) ; chrX:g.67722924T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722924T>A , CM000685.2:g.67722924T>A	GRCh38
NC_000023.10:g.66942766T>A , CM000685.1:g.66942766T>A	GRCh37
NC_000023.9:g.66859491T>A	NCBI36
NG_009014.2:g.183893T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*895T>A	ENSP00000379358.4:n.*895T>A
ENST00000374690.9:c.2547T>A MANE Select	ENSP00000363822.3:p.Asn849Lys
ENST00000396043.3:c.1174T>A	ENSP00000379358.3:n.1174T>A
ENST00000396044.8:c.2174-762T>A	ENSP00000379359.3:n.2174-762T>A
ENST00000612452.5:c.2547T>A	ENSP00000484033.2:p.Asn849Lys
ENST00000374690.7:c.2547T>A	ENSP00000363822.3:p.Asn849Lys
ENST00000396043.2:c.951T>A	ENSP00000379358.2:p.Asn317Lys
ENST00000396044.7:c.2174-762T>A	ENSP00000379359.3:n.2174-762T>A
ENST00000612452.4:c.1998T>A	ENSP00000484033.1:p.Asn666Lys
NM_000044.3:c.2547T>A	NP_000035.2:p.Asn849Lys
NM_001011645.2:c.951T>A	NP_001011645.1:p.Asn317Lys
NM_000044.4:c.2547T>A	NP_000035.2:p.Asn849Lys
NM_001011645.3:c.951T>A	NP_001011645.1:p.Asn317Lys
NM_000044.6:c.2547T>A MANE Select	NP_000035.2:p.Asn849Lys