Canonical Allele Identifier: CA120758

Gene: AR

Linked Data

• ClinVar Variation Id: 9838
• ClinVar RCV Id: RCV000010512
• dbSNP Id: rs137852586
• MyVariant Identifiers: chrX:g.66863220G>T (hg19) ; chrX:g.67643378G>T (hg38)
• PubMed: PMID:3216866 ; PMID:8809734

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67643378G>T , CM000685.2:g.67643378G>T	GRCh38
NC_000023.10:g.66863220G>T , CM000685.1:g.66863220G>T	GRCh37
NC_000023.9:g.66779945G>T	NCBI36
NG_009014.2:g.104347G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*87G>T	ENSP00000379358.4:n.*87G>T
ENST00000374690.9:c.1739G>T MANE Select	ENSP00000363822.3:p.Cys580Phe
ENST00000396043.3:c.366G>T	ENSP00000379358.3:n.366G>T
ENST00000396044.8:c.1739G>T	ENSP00000379359.3:p.Cys580Phe
ENST00000612452.5:c.1739G>T	ENSP00000484033.2:p.Cys580Phe
ENST00000374690.7:c.1739G>T	ENSP00000363822.3:p.Cys580Phe
ENST00000396043.2:c.143G>T	ENSP00000379358.2:p.Cys48Phe
ENST00000396044.7:c.1739G>T	ENSP00000379359.3:p.Cys580Phe
ENST00000504326.5:c.1739G>T	ENSP00000421155.1:p.Cys580Phe
ENST00000513847.5:n.2066G>T
ENST00000514029.5:c.1739G>T	ENSP00000425199.1:p.Cys580Phe
ENST00000612010.4:c.1739G>T	ENSP00000482407.1:p.Cys580Phe
ENST00000612452.4:c.1169G>T	ENSP00000484033.1:p.Cys390Phe
ENST00000613054.2:c.1617-42563G>T	ENSP00000479013.1:n.1617-42563G>T
NM_000044.3:c.1739G>T	NP_000035.2:p.Cys580Phe
NM_001011645.2:c.143G>T	NP_001011645.1:p.Cys48Phe
NM_000044.4:c.1739G>T	NP_000035.2:p.Cys580Phe
NM_001011645.3:c.143G>T	NP_001011645.1:p.Cys48Phe
NM_001348061.1:c.1739G>T	NP_001334990.1:p.Cys580Phe
NM_001348063.1:c.1739G>T	NP_001334992.1:p.Cys580Phe
NM_001348064.1:c.1617-42563G>T	NP_001334993.1:n.1617-42563G>T
NM_000044.6:c.1739G>T MANE Select	NP_000035.2:p.Cys580Phe