Canonical Allele Identifier: CA358687
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 9815
ClinVar RCV Id: RCV000010489
dbSNP Id: rs869320731

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545326_67545327del , CM000685.2:g.67545326_67545327del GRCh38
NC_000023.10:g.66765168_66765169del , CM000685.1:g.66765168_66765169del GRCh37
NC_000023.9:g.66681893_66681894del NCBI36
NG_009014.2:g.6295_6296del

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.180_181del ENSP00000379358.4:p.Gln61AlafsTer22
ENST00000374690.9:c.180_181del MANE Select ENSP00000363822.3:p.Gln61AlafsTer22
ENST00000396044.8:c.180_181del ENSP00000379359.3:p.Gln61AlafsTer22
ENST00000612452.5:c.180_181del ENSP00000484033.2:p.Gln61AlafsTer22
ENST00000374690.7:c.180_181del ENSP00000363822.3:p.Gln61AlafsTer22
ENST00000396044.7:c.180_181del ENSP00000379359.3:p.Gln61AlafsTer22
ENST00000504326.5:c.180_181del ENSP00000421155.1:p.Gln61AlafsTer22
ENST00000513847.5:n.507_508del
ENST00000514029.5:c.180_181del ENSP00000425199.1:p.Gln61AlafsTer22
ENST00000612010.4:c.180_181del ENSP00000482407.1:p.Gln61AlafsTer22
ENST00000612452.4:c.-391_-390del ENSP00000484033.1:n.-391_-390del
ENST00000613054.2:c.180_181del ENSP00000479013.1:p.Gln61AlafsTer22
NM_000044.3:c.180_181del NP_000035.2:p.Gln61AlafsTer22
NM_000044.4:c.180_181del NP_000035.2:p.Gln61AlafsTer22
NM_001011645.3:c.-1604_-1603del NP_001011645.1:n.-1604_-1603del
NM_001348061.1:c.180_181del NP_001334990.1:p.Gln61AlafsTer22
NM_001348063.1:c.180_181del NP_001334992.1:p.Gln61AlafsTer22
NM_001348064.1:c.180_181del NP_001334993.1:p.Gln61AlafsTer22
NM_000044.6:c.180_181del MANE Select NP_000035.2:p.Gln61AlafsTer22