Canonical Allele Identifier: CA2695224398
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67546008_67546015del , CM000685.2:g.67546008_67546015del GRCh38
NC_000023.10:g.66765850_66765857del , CM000685.1:g.66765850_66765857del GRCh37
NC_000023.9:g.66682575_66682582del NCBI36
NG_009014.2:g.6977_6984del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.862_869del ENSP00000379358.4:p.Ala288GlnfsTer14
ENST00000374690.9:c.862_869del MANE Select ENSP00000363822.3:p.Ala288GlnfsTer14
ENST00000396044.8:c.862_869del ENSP00000379359.3:p.Ala288GlnfsTer14
ENST00000612452.5:c.862_869del ENSP00000484033.2:p.Ala288GlnfsTer14
ENST00000374690.7:c.862_869del ENSP00000363822.3:p.Ala288GlnfsTer14
ENST00000396044.7:c.862_869del ENSP00000379359.3:p.Ala288GlnfsTer14
ENST00000504326.5:c.862_869del ENSP00000421155.1:p.Ala288GlnfsTer14
ENST00000513847.5:n.1189_1196del
ENST00000514029.5:c.862_869del ENSP00000425199.1:p.Ala288GlnfsTer14
ENST00000612010.4:c.862_869del ENSP00000482407.1:p.Ala288GlnfsTer14
ENST00000612452.4:c.292_299del ENSP00000484033.1:p.Ala98GlnfsTer14
ENST00000613054.2:c.862_869del ENSP00000479013.1:p.Ala288GlnfsTer14
NM_000044.3:c.862_869del NP_000035.2:p.Ala288GlnfsTer14
NM_000044.4:c.862_869del NP_000035.2:p.Ala288GlnfsTer14
NM_001011645.3:c.-922_-915del NP_001011645.1:n.-922_-915del
NM_001348061.1:c.862_869del NP_001334990.1:p.Ala288GlnfsTer14
NM_001348063.1:c.862_869del NP_001334992.1:p.Ala288GlnfsTer14
NM_001348064.1:c.862_869del NP_001334993.1:p.Ala288GlnfsTer14
NM_000044.6:c.862_869del MANE Select NP_000035.2:p.Ala288GlnfsTer14