Canonical Allele Identifier: CA16602789
Gene: AR HGNC NCBI

Linked Data

ClinVar Variation Id: 376347
ClinVar RCV Id: RCV003766181
dbSNP Id: rs1057519864
COSMIC: COSM5945752
MyVariant Identifiers: chrX:g.66943549T>C (hg19) chrX:g.67723707T>C (hg38)
CIViC: CA16602789
PubMed: PMID:23779130
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67723707T>C , CM000685.2:g.67723707T>C GRCh38
NC_000023.10:g.66943549T>C , CM000685.1:g.66943549T>C GRCh37
NC_000023.9:g.66860274T>C NCBI36
NG_009014.2:g.184676T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*977T>C ENSP00000379358.4:n.*977T>C
ENST00000374690.9:c.2629T>C MANE Select ENSP00000363822.3:p.Phe877Leu
ENST00000396043.3:c.1256T>C ENSP00000379358.3:n.1256T>C
ENST00000396044.8:c.2195T>C ENSP00000379359.3:p.Val732Ala
ENST00000612452.5:c.2629T>C ENSP00000484033.2:p.Phe877Leu
ENST00000374690.7:c.2629T>C ENSP00000363822.3:p.Phe877Leu
ENST00000396043.2:c.1033T>C ENSP00000379358.2:p.Phe345Leu
ENST00000396044.7:c.2195T>C ENSP00000379359.3:p.Val732Ala
ENST00000612452.4:c.2080T>C ENSP00000484033.1:p.Phe694Leu
NM_000044.3:c.2629T>C NP_000035.2:p.Phe877Leu
NM_001011645.2:c.1033T>C NP_001011645.1:p.Phe345Leu
NM_000044.4:c.2629T>C NP_000035.2:p.Phe877Leu
NM_001011645.3:c.1033T>C NP_001011645.1:p.Phe345Leu
NM_000044.6:c.2629T>C MANE Select NP_000035.2:p.Phe877Leu
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