Canonical Allele Identifier: CA2821614872

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711593_67711594insCCAA , CM000685.2:g.67711593_67711594insCCAA	GRCh38
NC_000023.10:g.66931435_66931436insCCAA , CM000685.1:g.66931435_66931436insCCAA	GRCh37
NC_000023.9:g.66848160_66848161insCCAA	NCBI36
NG_009014.2:g.172562_172563insCCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*425_*426insCCAA	ENSP00000379358.4:n.*425_*426insCCAA
ENST00000374690.9:c.2077_2078insCCAA MANE Select	ENSP00000363822.3:p.Asn693ThrfsTer13
ENST00000396043.3:c.704_705insCCAA	ENSP00000379358.3:n.704_705insCCAA
ENST00000396044.8:c.2077_2078insCCAA	ENSP00000379359.3:p.Asn693ThrfsTer13
ENST00000612452.5:c.2077_2078insCCAA	ENSP00000484033.2:p.Asn693ThrfsTer13
ENST00000374690.7:c.2077_2078insCCAA	ENSP00000363822.3:p.Asn693ThrfsTer13
ENST00000396043.2:c.481_482insCCAA	ENSP00000379358.2:p.Asn161ThrfsTer13
ENST00000396044.7:c.2077_2078insCCAA	ENSP00000379359.3:p.Asn693ThrfsTer13
ENST00000612452.4:c.1507_1508insCCAA	ENSP00000484033.1:p.Asn503ThrfsTer13
NM_000044.3:c.2077_2078insCCAA	NP_000035.2:p.Asn693ThrfsTer13
NM_001011645.2:c.481_482insCCAA	NP_001011645.1:p.Asn161ThrfsTer13
NM_000044.4:c.2077_2078insCCAA	NP_000035.2:p.Asn693ThrfsTer13
NM_001011645.3:c.481_482insCCAA	NP_001011645.1:p.Asn161ThrfsTer13
NM_000044.6:c.2077_2078insCCAA MANE Select	NP_000035.2:p.Asn693ThrfsTer13