Canonical Allele Identifier: CA2573158999

Gene: AR

Linked Data

• ClinVar Variation Id: 1518028
• ClinVar RCV Id: RCV002021449
• dbSNP Id: rs2147540838

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723828del , CM000685.2:g.67723828del	GRCh38
NC_000023.10:g.66943670del , CM000685.1:g.66943670del	GRCh37
NC_000023.9:g.66860395del	NCBI36
NG_009014.2:g.184797del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1098del	ENSP00000379358.4:n.*1098del
ENST00000374690.9:c.2750del MANE Select	ENSP00000363822.3:p.Phe917SerfsTer27
ENST00000396043.3:c.1377del	ENSP00000379358.3:n.1377del
ENST00000396044.8:c.*111del	ENSP00000379359.3:n.*111del
ENST00000612452.5:c.2750del	ENSP00000484033.2:p.Phe917SerfsTer27
ENST00000374690.7:c.2750del	ENSP00000363822.3:p.Phe917SerfsTer27
ENST00000396043.2:c.1154del	ENSP00000379358.2:p.Phe385SerfsTer27
ENST00000396044.7:c.*111del	ENSP00000379359.3:n.*111del
ENST00000612452.4:c.2201del	ENSP00000484033.1:p.Phe734SerfsTer27
NM_000044.3:c.2750del	NP_000035.2:p.Phe917SerfsTer27
NM_001011645.2:c.1154del	NP_001011645.1:p.Phe385SerfsTer27
NM_000044.4:c.2750del	NP_000035.2:p.Phe917SerfsTer27
NM_001011645.3:c.1154del	NP_001011645.1:p.Phe385SerfsTer27
NM_000044.6:c.2750del MANE Select	NP_000035.2:p.Phe917SerfsTer27