Canonical Allele Identifier: CA413427431

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942669T>C (hg19) ; chrX:g.67722827T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722827T>C , CM000685.2:g.67722827T>C	GRCh38
NC_000023.10:g.66942669T>C , CM000685.1:g.66942669T>C	GRCh37
NC_000023.9:g.66859394T>C	NCBI36
NG_009014.2:g.183796T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*798T>C	ENSP00000379358.4:n.*798T>C
ENST00000374690.9:c.2450T>C MANE Select	ENSP00000363822.3:p.Ile817Thr
ENST00000396043.3:c.1077T>C	ENSP00000379358.3:n.1077T>C
ENST00000396044.8:c.2174-859T>C	ENSP00000379359.3:n.2174-859T>C
ENST00000612452.5:c.2450T>C	ENSP00000484033.2:p.Ile817Thr
ENST00000374690.7:c.2450T>C	ENSP00000363822.3:p.Ile817Thr
ENST00000396043.2:c.854T>C	ENSP00000379358.2:p.Ile285Thr
ENST00000396044.7:c.2174-859T>C	ENSP00000379359.3:n.2174-859T>C
ENST00000612452.4:c.1901T>C	ENSP00000484033.1:p.Ile634Thr
NM_000044.3:c.2450T>C	NP_000035.2:p.Ile817Thr
NM_001011645.2:c.854T>C	NP_001011645.1:p.Ile285Thr
NM_000044.4:c.2450T>C	NP_000035.2:p.Ile817Thr
NM_001011645.3:c.854T>C	NP_001011645.1:p.Ile285Thr
NM_000044.6:c.2450T>C MANE Select	NP_000035.2:p.Ile817Thr