Canonical Allele Identifier: CA2821614873
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67711595_67711596insACACCCAACA , CM000685.2:g.67711595_67711596insACACCCAACA GRCh38
NC_000023.10:g.66931437_66931438insACACCCAACA , CM000685.1:g.66931437_66931438insACACCCAACA GRCh37
NC_000023.9:g.66848162_66848163insACACCCAACA NCBI36
NG_009014.2:g.172564_172565insACACCCAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*427_*428insACACCCAACA ENSP00000379358.4:n.*427_*428insACACCCAACA
ENST00000374690.9:c.2079_2080insACACCCAACA MANE Select ENSP00000363822.3:p.Gln694ThrfsTer14
ENST00000396043.3:c.706_707insACACCCAACA ENSP00000379358.3:n.706_707insACACCCAACA
ENST00000396044.8:c.2079_2080insACACCCAACA ENSP00000379359.3:p.Gln694ThrfsTer14
ENST00000612452.5:c.2079_2080insACACCCAACA ENSP00000484033.2:p.Gln694ThrfsTer14
ENST00000374690.7:c.2079_2080insACACCCAACA ENSP00000363822.3:p.Gln694ThrfsTer14
ENST00000396043.2:c.483_484insACACCCAACA ENSP00000379358.2:p.Gln162ThrfsTer14
ENST00000396044.7:c.2079_2080insACACCCAACA ENSP00000379359.3:p.Gln694ThrfsTer14
ENST00000612452.4:c.1509_1510insACACCCAACA ENSP00000484033.1:p.Gln504ThrfsTer14
NM_000044.3:c.2079_2080insACACCCAACA NP_000035.2:p.Gln694ThrfsTer14
NM_001011645.2:c.483_484insACACCCAACA NP_001011645.1:p.Gln162ThrfsTer14
NM_000044.4:c.2079_2080insACACCCAACA NP_000035.2:p.Gln694ThrfsTer14
NM_001011645.3:c.483_484insACACCCAACA NP_001011645.1:p.Gln162ThrfsTer14
NM_000044.6:c.2079_2080insACACCCAACA MANE Select NP_000035.2:p.Gln694ThrfsTer14