Canonical Allele Identifier: CA517048726

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66931530T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711688T>G , CM000685.2:g.67711688T>G	GRCh38
NC_000023.10:g.66931530T>G , CM000685.1:g.66931530T>G	GRCh37
NC_000023.9:g.66848255T>G	NCBI36
NG_009014.2:g.172657T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*520T>G	ENSP00000379358.4:n.*520T>G
ENST00000374690.9:c.2172T>G MANE Select	ENSP00000363822.3:p.Pro724=
ENST00000396043.3:c.799T>G	ENSP00000379358.3:n.799T>G
ENST00000396044.8:c.2172T>G	ENSP00000379359.3:p.Pro724=
ENST00000612452.5:c.2172T>G	ENSP00000484033.2:p.Pro724=
ENST00000374690.7:c.2172T>G	ENSP00000363822.3:p.Pro724=
ENST00000396043.2:c.576T>G	ENSP00000379358.2:p.Pro192=
ENST00000396044.7:c.2172T>G	ENSP00000379359.3:p.Pro724=
ENST00000612452.4:c.1602T>G	ENSP00000484033.1:p.Pro534=
NM_000044.3:c.2172T>G	NP_000035.2:p.Pro724=
NM_001011645.2:c.576T>G	NP_001011645.1:p.Pro192=
NM_000044.4:c.2172T>G	NP_000035.2:p.Pro724=
NM_001011645.3:c.576T>G	NP_001011645.1:p.Pro192=
NM_000044.6:c.2172T>G MANE Select	NP_000035.2:p.Pro724=