Canonical Allele Identifier: CA10436670

Gene: AR

Linked Data

• dbSNP Id: rs775502238
• ExAC: X:66942750 C / T
• gnomAD v2: X-66942750-C-T
• gnomAD v4: X-67722908-C-T
• MyVariant Identifiers: chrX:g.66942750C>T (hg19) ; chrX:g.67722908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722908C>T , CM000685.2:g.67722908C>T	GRCh38
NC_000023.10:g.66942750C>T , CM000685.1:g.66942750C>T	GRCh37
NC_000023.9:g.66859475C>T	NCBI36
NG_009014.2:g.183877C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*879C>T	ENSP00000379358.4:n.*879C>T
ENST00000374690.9:c.2531C>T MANE Select	ENSP00000363822.3:p.Ala844Val
ENST00000396043.3:c.1158C>T	ENSP00000379358.3:n.1158C>T
ENST00000396044.8:c.2174-778C>T	ENSP00000379359.3:n.2174-778C>T
ENST00000612452.5:c.2531C>T	ENSP00000484033.2:p.Ala844Val
ENST00000374690.7:c.2531C>T	ENSP00000363822.3:p.Ala844Val
ENST00000396043.2:c.935C>T	ENSP00000379358.2:p.Ala312Val
ENST00000396044.7:c.2174-778C>T	ENSP00000379359.3:n.2174-778C>T
ENST00000612452.4:c.1982C>T	ENSP00000484033.1:p.Ala661Val
NM_000044.3:c.2531C>T	NP_000035.2:p.Ala844Val
NM_001011645.2:c.935C>T	NP_001011645.1:p.Ala312Val
NM_000044.4:c.2531C>T	NP_000035.2:p.Ala844Val
NM_001011645.3:c.935C>T	NP_001011645.1:p.Ala312Val
NM_000044.6:c.2531C>T MANE Select	NP_000035.2:p.Ala844Val