Canonical Allele Identifier: CA16043328
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 373055
ClinVar RCV Id: RCV000414028
dbSNP Id: rs1057518177
MyVariant Identifiers: chrX:g.66931397_66931414del (hg19) chrX:g.67711555_67711572del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67711555_67711572del , CM000685.2:g.67711555_67711572del GRCh38
NC_000023.10:g.66931397_66931414del , CM000685.1:g.66931397_66931414del GRCh37
NC_000023.9:g.66848122_66848139del NCBI36
NG_009014.2:g.172524_172541del

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*387_*404del ENSP00000379358.4:n.*387_*404del
ENST00000374690.9:c.2039_2056del MANE Select ENSP00000363822.3:p.Ala680_Val685del
ENST00000396043.3:c.666_683del ENSP00000379358.3:n.666_683del
ENST00000396044.8:c.2039_2056del ENSP00000379359.3:p.Ala680_Val685del
ENST00000612452.5:c.2039_2056del ENSP00000484033.2:p.Ala680_Val685del
ENST00000374690.7:c.2039_2056del ENSP00000363822.3:p.Ala680_Val685del
ENST00000396043.2:c.443_460del ENSP00000379358.2:p.Ala148_Val153del
ENST00000396044.7:c.2039_2056del ENSP00000379359.3:p.Ala680_Val685del
ENST00000612452.4:c.1469_1486del ENSP00000484033.1:p.Ala490_Val495del
NM_000044.3:c.2039_2056del NP_000035.2:p.Ala680_Val685del
NM_001011645.2:c.443_460del NP_001011645.1:p.Ala148_Val153del
NM_000044.4:c.2039_2056del NP_000035.2:p.Ala680_Val685del
NM_001011645.3:c.443_460del NP_001011645.1:p.Ala148_Val153del
NM_000044.6:c.2039_2056del MANE Select NP_000035.2:p.Ala680_Val685del
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