Canonical Allele Identifier: CA120686

Gene: AR

Linked Data

• ClinVar Variation Id: 9807
• ClinVar RCV Id: RCV000010481 ; RCV000698414
• dbSNP Id: rs137852565
• COSMIC: COSM1558413 ; COSM6187571 ; COSM6187572
• MyVariant Identifiers: chrX:g.66941747G>A (hg19) ; chrX:g.67721905G>A (hg38)
• PubMed: PMID:2332504

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721905G>A , CM000685.2:g.67721905G>A	GRCh38
NC_000023.10:g.66941747G>A , CM000685.1:g.66941747G>A	GRCh37
NC_000023.9:g.66858472G>A	NCBI36
NG_009014.2:g.182874G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*739G>A	ENSP00000379358.4:n.*739G>A
ENST00000374690.9:c.2391G>A MANE Select	ENSP00000363822.3:p.Trp797Ter
ENST00000396043.3:c.1018G>A	ENSP00000379358.3:n.1018G>A
ENST00000396044.8:c.2174-1781G>A	ENSP00000379359.3:n.2174-1781G>A
ENST00000612452.5:c.2391G>A	ENSP00000484033.2:p.Trp797Ter
ENST00000374690.7:c.2391G>A	ENSP00000363822.3:p.Trp797Ter
ENST00000396043.2:c.795G>A	ENSP00000379358.2:p.Trp265Ter
ENST00000396044.7:c.2174-1781G>A	ENSP00000379359.3:n.2174-1781G>A
ENST00000612452.4:c.1821G>A	ENSP00000484033.1:p.Trp607Ter
NM_000044.3:c.2391G>A	NP_000035.2:p.Trp797Ter
NM_001011645.2:c.795G>A	NP_001011645.1:p.Trp265Ter
NM_000044.4:c.2391G>A	NP_000035.2:p.Trp797Ter
NM_001011645.3:c.795G>A	NP_001011645.1:p.Trp265Ter
NM_000044.6:c.2391G>A MANE Select	NP_000035.2:p.Trp797Ter