Canonical Allele Identifier: CA10436610

Gene: AR

Linked Data

• ClinVar Variation Id: 2946277
• ClinVar RCV Id: RCV003806563
• dbSNP Id: rs369390411
• ExAC: X:66937441 C / T
• gnomAD v2: X-66937441-C-T
• gnomAD v3: X-67717599-C-T
• gnomAD v4: X-67717599-C-T
• COSMIC: COSM3406531 ; COSM3406532
• MyVariant Identifiers: chrX:g.66937441C>T (hg19) ; chrX:g.67717599C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717599C>T , CM000685.2:g.67717599C>T	GRCh38
NC_000023.10:g.66937441C>T , CM000685.1:g.66937441C>T	GRCh37
NC_000023.9:g.66854166C>T	NCBI36
NG_009014.2:g.178568C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*643C>T	ENSP00000379358.4:n.*643C>T
ENST00000374690.9:c.2295C>T MANE Select	ENSP00000363822.3:p.Phe765=
ENST00000396043.3:c.922C>T	ENSP00000379358.3:n.922C>T
ENST00000396044.8:c.2173+5910C>T	ENSP00000379359.3:n.2173+5910C>T
ENST00000612452.5:c.2295C>T	ENSP00000484033.2:p.Phe765=
ENST00000374690.7:c.2295C>T	ENSP00000363822.3:p.Phe765=
ENST00000396043.2:c.699C>T	ENSP00000379358.2:p.Phe233=
ENST00000396044.7:c.2173+5910C>T	ENSP00000379359.3:n.2173+5910C>T
ENST00000612452.4:c.1725C>T	ENSP00000484033.1:p.Phe575=
NM_000044.3:c.2295C>T	NP_000035.2:p.Phe765=
NM_001011645.2:c.699C>T	NP_001011645.1:p.Phe233=
NM_000044.4:c.2295C>T	NP_000035.2:p.Phe765=
NM_001011645.3:c.699C>T	NP_001011645.1:p.Phe233=
NM_000044.6:c.2295C>T MANE Select	NP_000035.2:p.Phe765=