Canonical Allele Identifier: CA413428235
Gene: AR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723725A>G , CM000685.2:g.67723725A>G GRCh38
NC_000023.10:g.66943567A>G , CM000685.1:g.66943567A>G GRCh37
NC_000023.9:g.66860292A>G NCBI36
NG_009014.2:g.184694A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*995A>G ENSP00000379358.4:n.*995A>G
ENST00000374690.9:c.2647A>G MANE Select ENSP00000363822.3:p.Ile883Val
ENST00000396043.3:c.1274A>G ENSP00000379358.3:n.1274A>G
ENST00000396044.8:c.*8A>G ENSP00000379359.3:n.*8A>G
ENST00000612452.5:c.2647A>G ENSP00000484033.2:p.Ile883Val
ENST00000374690.7:c.2647A>G ENSP00000363822.3:p.Ile883Val
ENST00000396043.2:c.1051A>G ENSP00000379358.2:p.Ile351Val
ENST00000396044.7:c.*8A>G ENSP00000379359.3:n.*8A>G
ENST00000612452.4:c.2098A>G ENSP00000484033.1:p.Ile700Val
NM_000044.3:c.2647A>G NP_000035.2:p.Ile883Val
NM_001011645.2:c.1051A>G NP_001011645.1:p.Ile351Val
NM_000044.4:c.2647A>G NP_000035.2:p.Ile883Val
NM_001011645.3:c.1051A>G NP_001011645.1:p.Ile351Val
NM_000044.6:c.2647A>G MANE Select NP_000035.2:p.Ile883Val
Search 100 bp 5'
Search 100 bp 3'