Canonical Allele Identifier: CA413427882

Gene: AR

Linked Data

• dbSNP Id: rs1419690127
• gnomAD v2: X-66942737-G-A
• gnomAD v4: X-67722895-G-A
• COSMIC: COSM93906
• MyVariant Identifiers: chrX:g.66942737G>A (hg19) ; chrX:g.67722895G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722895G>A , CM000685.2:g.67722895G>A	GRCh38
NC_000023.10:g.66942737G>A , CM000685.1:g.66942737G>A	GRCh37
NC_000023.9:g.66859462G>A	NCBI36
NG_009014.2:g.183864G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*866G>A	ENSP00000379358.4:n.*866G>A
ENST00000374690.9:c.2518G>A MANE Select	ENSP00000363822.3:p.Asp840Asn
ENST00000396043.3:c.1145G>A	ENSP00000379358.3:n.1145G>A
ENST00000396044.8:c.2174-791G>A	ENSP00000379359.3:n.2174-791G>A
ENST00000612452.5:c.2518G>A	ENSP00000484033.2:p.Asp840Asn
ENST00000374690.7:c.2518G>A	ENSP00000363822.3:p.Asp840Asn
ENST00000396043.2:c.922G>A	ENSP00000379358.2:p.Asp308Asn
ENST00000396044.7:c.2174-791G>A	ENSP00000379359.3:n.2174-791G>A
ENST00000612452.4:c.1969G>A	ENSP00000484033.1:p.Asp657Asn
NM_000044.3:c.2518G>A	NP_000035.2:p.Asp840Asn
NM_001011645.2:c.922G>A	NP_001011645.1:p.Asp308Asn
NM_000044.4:c.2518G>A	NP_000035.2:p.Asp840Asn
NM_001011645.3:c.922G>A	NP_001011645.1:p.Asp308Asn
NM_000044.6:c.2518G>A MANE Select	NP_000035.2:p.Asp840Asn