Canonical Allele Identifier: CA2738684744
Gene: AR HGNC NCBI

Linked Data

dbSNP Id: rs2147319136

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67546065_67546066del , CM000685.2:g.67546065_67546066del GRCh38
NC_000023.10:g.66765907_66765908del , CM000685.1:g.66765907_66765908del GRCh37
NC_000023.9:g.66682632_66682633del NCBI36
NG_009014.2:g.7034_7035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.919_920del ENSP00000379358.4:p.Ala307Ter
ENST00000374690.9:c.919_920del MANE Select ENSP00000363822.3:p.Ala307Ter
ENST00000396044.8:c.919_920del ENSP00000379359.3:p.Ala307Ter
ENST00000612452.5:c.919_920del ENSP00000484033.2:p.Ala307Ter
ENST00000374690.7:c.919_920del ENSP00000363822.3:p.Ala307Ter
ENST00000396044.7:c.919_920del ENSP00000379359.3:p.Ala307Ter
ENST00000504326.5:c.919_920del ENSP00000421155.1:p.Ala307Ter
ENST00000513847.5:n.1246_1247del
ENST00000514029.5:c.919_920del ENSP00000425199.1:p.Ala307Ter
ENST00000612010.4:c.919_920del ENSP00000482407.1:p.Ala307Ter
ENST00000612452.4:c.349_350del ENSP00000484033.1:p.Ala117Ter
ENST00000613054.2:c.919_920del ENSP00000479013.1:p.Ala307Ter
NM_000044.3:c.919_920del NP_000035.2:p.Ala307Ter
NM_000044.4:c.919_920del NP_000035.2:p.Ala307Ter
NM_001011645.3:c.-865_-864del NP_001011645.1:n.-865_-864del
NM_001348061.1:c.919_920del NP_001334990.1:p.Ala307Ter
NM_001348063.1:c.919_920del NP_001334992.1:p.Ala307Ter
NM_001348064.1:c.919_920del NP_001334993.1:p.Ala307Ter
NM_000044.6:c.919_920del MANE Select NP_000035.2:p.Ala307Ter