Canonical Allele Identifier: CA915951141

Gene: AR

Linked Data

• ClinVar Variation Id: 642559
• ClinVar RCV Id: RCV000796043
• dbSNP Id: rs1602280414

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723830del , CM000685.2:g.67723830del	GRCh38
NC_000023.10:g.66943672del , CM000685.1:g.66943672del	GRCh37
NC_000023.9:g.66860397del	NCBI36
NG_009014.2:g.184799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1100del	ENSP00000379358.4:n.*1100del
ENST00000374690.9:c.2752del MANE Select	ENSP00000363822.3:p.His918ThrfsTer26
ENST00000396043.3:c.1379del	ENSP00000379358.3:n.1379del
ENST00000396044.8:c.*113del	ENSP00000379359.3:n.*113del
ENST00000612452.5:c.2752del	ENSP00000484033.2:p.His918ThrfsTer26
ENST00000374690.7:c.2752del	ENSP00000363822.3:p.His918ThrfsTer26
ENST00000396043.2:c.1156del	ENSP00000379358.2:p.His386ThrfsTer26
ENST00000396044.7:c.*113del	ENSP00000379359.3:n.*113del
ENST00000612452.4:c.2203del	ENSP00000484033.1:p.His735ThrfsTer26
NM_000044.3:c.2752del	NP_000035.2:p.His918ThrfsTer26
NM_001011645.2:c.1156del	NP_001011645.1:p.His386ThrfsTer26
NM_000044.4:c.2752del	NP_000035.2:p.His918ThrfsTer26
NM_001011645.3:c.1156del	NP_001011645.1:p.His386ThrfsTer26
NM_000044.6:c.2752del MANE Select	NP_000035.2:p.His918ThrfsTer26