Canonical Allele Identifier: CA2573055379
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 1338498
ClinVar RCV Id: RCV001817869
dbSNP Id: rs2147317782

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545821_67545824del , CM000685.2:g.67545821_67545824del GRCh38
NC_000023.10:g.66765663_66765666del , CM000685.1:g.66765663_66765666del GRCh37
NC_000023.9:g.66682388_66682391del NCBI36
NG_009014.2:g.6790_6793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.675_678del ENSP00000379358.4:p.Tyr225Ter
ENST00000374690.9:c.675_678del MANE Select ENSP00000363822.3:p.Tyr225Ter
ENST00000396044.8:c.675_678del ENSP00000379359.3:p.Tyr225Ter
ENST00000612452.5:c.675_678del ENSP00000484033.2:p.Tyr225Ter
ENST00000374690.7:c.675_678del ENSP00000363822.3:p.Tyr225Ter
ENST00000396044.7:c.675_678del ENSP00000379359.3:p.Tyr225Ter
ENST00000504326.5:c.675_678del ENSP00000421155.1:p.Tyr225Ter
ENST00000513847.5:n.1002_1005del
ENST00000514029.5:c.675_678del ENSP00000425199.1:p.Tyr225Ter
ENST00000612010.4:c.675_678del ENSP00000482407.1:p.Tyr225Ter
ENST00000612452.4:c.105_108del ENSP00000484033.1:p.Tyr35Ter
ENST00000613054.2:c.675_678del ENSP00000479013.1:p.Tyr225Ter
NM_000044.3:c.675_678del NP_000035.2:p.Tyr225Ter
NM_000044.4:c.675_678del NP_000035.2:p.Tyr225Ter
NM_001011645.3:c.-1109_-1106del NP_001011645.1:n.-1109_-1106del
NM_001348061.1:c.675_678del NP_001334990.1:p.Tyr225Ter
NM_001348063.1:c.675_678del NP_001334992.1:p.Tyr225Ter
NM_001348064.1:c.675_678del NP_001334993.1:p.Tyr225Ter
NM_000044.6:c.675_678del MANE Select NP_000035.2:p.Tyr225Ter