Canonical Allele Identifier: CA10436527

Gene: AR

Linked Data

• ClinVar Variation Id: 2931825
• ClinVar RCV Id: RCV003792847
• dbSNP Id: rs151266937
• ExAC: X:66905937 G / A
• gnomAD v2: X-66905937-G-A
• gnomAD v3: X-67686095-G-A
• gnomAD v4: X-67686095-G-A
• MyVariant Identifiers: chrX:g.66905937G>A (hg19) ; chrX:g.67686095G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686095G>A , CM000685.2:g.67686095G>A	GRCh38
NC_000023.10:g.66905937G>A , CM000685.1:g.66905937G>A	GRCh37
NC_000023.9:g.66822662G>A	NCBI36
NG_009014.2:g.147064G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*202G>A	ENSP00000379358.4:n.*202G>A
ENST00000374690.9:c.1854G>A MANE Select	ENSP00000363822.3:p.Arg618=
ENST00000396043.3:c.481G>A	ENSP00000379358.3:n.481G>A
ENST00000396044.8:c.1854G>A	ENSP00000379359.3:p.Arg618=
ENST00000612452.5:c.1854G>A	ENSP00000484033.2:p.Arg618=
ENST00000374690.7:c.1854G>A	ENSP00000363822.3:p.Arg618=
ENST00000396043.2:c.258G>A	ENSP00000379358.2:p.Arg86=
ENST00000396044.7:c.1854G>A	ENSP00000379359.3:p.Arg618=
ENST00000504326.5:c.1854G>A	ENSP00000421155.1:p.Arg618=
ENST00000513847.5:n.2181G>A
ENST00000514029.5:c.*335G>A	ENSP00000425199.1:n.*335G>A
ENST00000612010.4:c.*206G>A	ENSP00000482407.1:n.*206G>A
ENST00000612452.4:c.1284G>A	ENSP00000484033.1:p.Arg428=
ENST00000613054.2:c.*52G>A	ENSP00000479013.1:n.*52G>A
NM_000044.3:c.1854G>A	NP_000035.2:p.Arg618=
NM_001011645.2:c.258G>A	NP_001011645.1:p.Arg86=
NM_000044.4:c.1854G>A	NP_000035.2:p.Arg618=
NM_001011645.3:c.258G>A	NP_001011645.1:p.Arg86=
NM_001348061.1:c.1854G>A	NP_001334990.1:p.Arg618=
NM_001348063.1:c.1854G>A	NP_001334992.1:p.Arg618=
NM_001348064.1:c.*52G>A	NP_001334993.1:n.*52G>A
NM_000044.6:c.1854G>A MANE Select	NP_000035.2:p.Arg618=