Canonical Allele Identifier: CA645603436

Gene: AR

Linked Data

• ClinVar Variation Id: 1344505
• ClinVar RCV Id: RCV001848601
• dbSNP Id: rs2147535891
• COSMIC: COSM4169447 ; COSM4169448

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721921dup , CM000685.2:g.67721921dup	GRCh38
NC_000023.10:g.66941763dup , CM000685.1:g.66941763dup	GRCh37
NC_000023.9:g.66858488dup	NCBI36
NG_009014.2:g.182890dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*755dup	ENSP00000379358.4:n.*755dup
ENST00000374690.9:c.2407dup MANE Select	ENSP00000363822.3:p.Gln803ProfsTer27
ENST00000396043.3:c.1034dup	ENSP00000379358.3:n.1034dup
ENST00000396044.8:c.2174-1765dup	ENSP00000379359.3:n.2174-1765dup
ENST00000612452.5:c.2407dup	ENSP00000484033.2:p.Gln803ProfsTer27
ENST00000374690.7:c.2407dup	ENSP00000363822.3:p.Gln803ProfsTer27
ENST00000396043.2:c.811dup	ENSP00000379358.2:p.Gln271ProfsTer27
ENST00000396044.7:c.2174-1765dup	ENSP00000379359.3:n.2174-1765dup
ENST00000612452.4:c.1837dup	ENSP00000484033.1:p.Gln613ProfsTer15
NM_000044.3:c.2407dup	NP_000035.2:p.Gln803ProfsTer27
NM_001011645.2:c.811dup	NP_001011645.1:p.Gln271ProfsTer27
NM_000044.4:c.2407dup	NP_000035.2:p.Gln803ProfsTer27
NM_001011645.3:c.811dup	NP_001011645.1:p.Gln271ProfsTer27
NM_000044.6:c.2407dup MANE Select	NP_000035.2:p.Gln803ProfsTer27