Canonical Allele Identifier: CA16621464
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 419102
ClinVar RCV Id: RCV000482936
dbSNP Id: rs1064793645
MyVariant Identifiers: chrX:g.66931310del (hg19) chrX:g.67711468del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67711468del , CM000685.2:g.67711468del GRCh38
NC_000023.10:g.66931310del , CM000685.1:g.66931310del GRCh37
NC_000023.9:g.66848035del NCBI36
NG_009014.2:g.172437del

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*300del ENSP00000379358.4:n.*300del
ENST00000374690.9:c.1952del MANE Select ENSP00000363822.3:p.Ser651ThrfsTer10
ENST00000396043.3:c.579del ENSP00000379358.3:n.579del
ENST00000396044.8:c.1952del ENSP00000379359.3:p.Ser651ThrfsTer10
ENST00000612452.5:c.1952del ENSP00000484033.2:p.Ser651ThrfsTer10
ENST00000374690.7:c.1952del ENSP00000363822.3:p.Ser651ThrfsTer10
ENST00000396043.2:c.356del ENSP00000379358.2:p.Ser119ThrfsTer10
ENST00000396044.7:c.1952del ENSP00000379359.3:p.Ser651ThrfsTer10
ENST00000612452.4:c.1382del ENSP00000484033.1:p.Ser461ThrfsTer10
NM_000044.3:c.1952del NP_000035.2:p.Ser651ThrfsTer10
NM_001011645.2:c.356del NP_001011645.1:p.Ser119ThrfsTer10
NM_000044.4:c.1952del NP_000035.2:p.Ser651ThrfsTer10
NM_001011645.3:c.356del NP_001011645.1:p.Ser119ThrfsTer10
NM_000044.6:c.1952del MANE Select NP_000035.2:p.Ser651ThrfsTer10
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