Canonical Allele Identifier: CA2740092185

Gene: AR

Linked Data

• ClinVar Variation Id: 3061398
• ClinVar RCV Id: RCV003983406

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723821del , CM000685.2:g.67723821del	GRCh38
NC_000023.10:g.66943663del , CM000685.1:g.66943663del	GRCh37
NC_000023.9:g.66860388del	NCBI36
NG_009014.2:g.184790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1091del	ENSP00000379358.4:n.*1091del
ENST00000374690.9:c.2743del MANE Select	ENSP00000363822.3:p.Ile915SerfsTer29
ENST00000396043.3:c.1370del	ENSP00000379358.3:n.1370del
ENST00000396044.8:c.*104del	ENSP00000379359.3:n.*104del
ENST00000612452.5:c.2743del	ENSP00000484033.2:p.Ile915SerfsTer29
ENST00000374690.7:c.2743del	ENSP00000363822.3:p.Ile915SerfsTer29
ENST00000396043.2:c.1147del	ENSP00000379358.2:p.Ile383SerfsTer29
ENST00000396044.7:c.*104del	ENSP00000379359.3:n.*104del
ENST00000612452.4:c.2194del	ENSP00000484033.1:p.Ile732SerfsTer29
NM_000044.3:c.2743del	NP_000035.2:p.Ile915SerfsTer29
NM_001011645.2:c.1147del	NP_001011645.1:p.Ile383SerfsTer29
NM_000044.4:c.2743del	NP_000035.2:p.Ile915SerfsTer29
NM_001011645.3:c.1147del	NP_001011645.1:p.Ile383SerfsTer29
NM_000044.6:c.2743del MANE Select	NP_000035.2:p.Ile915SerfsTer29