Canonical Allele Identifier: CA413423366

Gene: AR

Linked Data

• ClinVar Variation Id: 1333500
• ClinVar RCV Id: RCV001808188
• dbSNP Id: rs2147524940
• MyVariant Identifiers: chrX:g.66931436A>T (hg19) ; chrX:g.67711594A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711594A>T , CM000685.2:g.67711594A>T	GRCh38
NC_000023.10:g.66931436A>T , CM000685.1:g.66931436A>T	GRCh37
NC_000023.9:g.66848161A>T	NCBI36
NG_009014.2:g.172563A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*426A>T	ENSP00000379358.4:n.*426A>T
ENST00000374690.9:c.2078A>T MANE Select	ENSP00000363822.3:p.Asn693Ile
ENST00000396043.3:c.705A>T	ENSP00000379358.3:n.705A>T
ENST00000396044.8:c.2078A>T	ENSP00000379359.3:p.Asn693Ile
ENST00000612452.5:c.2078A>T	ENSP00000484033.2:p.Asn693Ile
ENST00000374690.7:c.2078A>T	ENSP00000363822.3:p.Asn693Ile
ENST00000396043.2:c.482A>T	ENSP00000379358.2:p.Asn161Ile
ENST00000396044.7:c.2078A>T	ENSP00000379359.3:p.Asn693Ile
ENST00000612452.4:c.1508A>T	ENSP00000484033.1:p.Asn503Ile
NM_000044.3:c.2078A>T	NP_000035.2:p.Asn693Ile
NM_001011645.2:c.482A>T	NP_001011645.1:p.Asn161Ile
NM_000044.4:c.2078A>T	NP_000035.2:p.Asn693Ile
NM_001011645.3:c.482A>T	NP_001011645.1:p.Asn161Ile
NM_000044.6:c.2078A>T MANE Select	NP_000035.2:p.Asn693Ile