Canonical Allele Identifier: CA10436526

Gene: AR

Linked Data

• dbSNP Id: rs759988495
• ExAC: X:66905936 G / A
• gnomAD v2: X-66905936-G-A
• gnomAD v3: X-67686094-G-A
• gnomAD v4: X-67686094-G-A
• MyVariant Identifiers: chrX:g.66905936G>A (hg19) ; chrX:g.67686094G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686094G>A , CM000685.2:g.67686094G>A	GRCh38
NC_000023.10:g.66905936G>A , CM000685.1:g.66905936G>A	GRCh37
NC_000023.9:g.66822661G>A	NCBI36
NG_009014.2:g.147063G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*201G>A	ENSP00000379358.4:n.*201G>A
ENST00000374690.9:c.1853G>A MANE Select	ENSP00000363822.3:p.Arg618Gln
ENST00000396043.3:c.480G>A	ENSP00000379358.3:n.480G>A
ENST00000396044.8:c.1853G>A	ENSP00000379359.3:p.Arg618Gln
ENST00000612452.5:c.1853G>A	ENSP00000484033.2:p.Arg618Gln
ENST00000374690.7:c.1853G>A	ENSP00000363822.3:p.Arg618Gln
ENST00000396043.2:c.257G>A	ENSP00000379358.2:p.Arg86Gln
ENST00000396044.7:c.1853G>A	ENSP00000379359.3:p.Arg618Gln
ENST00000504326.5:c.1853G>A	ENSP00000421155.1:p.Arg618Gln
ENST00000513847.5:n.2180G>A
ENST00000514029.5:c.*334G>A	ENSP00000425199.1:n.*334G>A
ENST00000612010.4:c.*205G>A	ENSP00000482407.1:n.*205G>A
ENST00000612452.4:c.1283G>A	ENSP00000484033.1:p.Arg428Gln
ENST00000613054.2:c.*51G>A	ENSP00000479013.1:n.*51G>A
NM_000044.3:c.1853G>A	NP_000035.2:p.Arg618Gln
NM_001011645.2:c.257G>A	NP_001011645.1:p.Arg86Gln
NM_000044.4:c.1853G>A	NP_000035.2:p.Arg618Gln
NM_001011645.3:c.257G>A	NP_001011645.1:p.Arg86Gln
NM_001348061.1:c.1853G>A	NP_001334990.1:p.Arg618Gln
NM_001348063.1:c.1853G>A	NP_001334992.1:p.Arg618Gln
NM_001348064.1:c.*51G>A	NP_001334993.1:n.*51G>A
NM_000044.6:c.1853G>A MANE Select	NP_000035.2:p.Arg618Gln