Canonical Allele Identifier: CA10436664

Gene: AR

Linked Data

• ClinVar Variation Id: 2925265
• ClinVar RCV Id: RCV003780919
• dbSNP Id: rs369196297
• ExAC: X:66942709 A / G
• gnomAD v2: X-66942709-A-G
• MyVariant Identifiers: chrX:g.66942709A>G (hg19) ; chrX:g.67722867A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722867A>G , CM000685.2:g.67722867A>G	GRCh38
NC_000023.10:g.66942709A>G , CM000685.1:g.66942709A>G	GRCh37
NC_000023.9:g.66859434A>G	NCBI36
NG_009014.2:g.183836A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*838A>G	ENSP00000379358.4:n.*838A>G
ENST00000374690.9:c.2490A>G MANE Select	ENSP00000363822.3:p.Glu830=
ENST00000396043.3:c.1117A>G	ENSP00000379358.3:n.1117A>G
ENST00000396044.8:c.2174-819A>G	ENSP00000379359.3:n.2174-819A>G
ENST00000612452.5:c.2490A>G	ENSP00000484033.2:p.Glu830=
ENST00000374690.7:c.2490A>G	ENSP00000363822.3:p.Glu830=
ENST00000396043.2:c.894A>G	ENSP00000379358.2:p.Glu298=
ENST00000396044.7:c.2174-819A>G	ENSP00000379359.3:n.2174-819A>G
ENST00000612452.4:c.1941A>G	ENSP00000484033.1:p.Glu647=
NM_000044.3:c.2490A>G	NP_000035.2:p.Glu830=
NM_001011645.2:c.894A>G	NP_001011645.1:p.Glu298=
NM_000044.4:c.2490A>G	NP_000035.2:p.Glu830=
NM_001011645.3:c.894A>G	NP_001011645.1:p.Glu298=
NM_000044.6:c.2490A>G MANE Select	NP_000035.2:p.Glu830=