Canonical Allele Identifier: CA516973437

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66943665C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723823C>A , CM000685.2:g.67723823C>A	GRCh38
NC_000023.10:g.66943665C>A , CM000685.1:g.66943665C>A	GRCh37
NC_000023.9:g.66860390C>A	NCBI36
NG_009014.2:g.184792C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1093C>A	ENSP00000379358.4:n.*1093C>A
ENST00000374690.9:c.2745C>A MANE Select	ENSP00000363822.3:p.Ile915=
ENST00000396043.3:c.1372C>A	ENSP00000379358.3:n.1372C>A
ENST00000396044.8:c.*106C>A	ENSP00000379359.3:n.*106C>A
ENST00000612452.5:c.2745C>A	ENSP00000484033.2:p.Ile915=
ENST00000374690.7:c.2745C>A	ENSP00000363822.3:p.Ile915=
ENST00000396043.2:c.1149C>A	ENSP00000379358.2:p.Ile383=
ENST00000396044.7:c.*106C>A	ENSP00000379359.3:n.*106C>A
ENST00000612452.4:c.2196C>A	ENSP00000484033.1:p.Ile732=
NM_000044.3:c.2745C>A	NP_000035.2:p.Ile915=
NM_001011645.2:c.1149C>A	NP_001011645.1:p.Ile383=
NM_000044.4:c.2745C>A	NP_000035.2:p.Ile915=
NM_001011645.3:c.1149C>A	NP_001011645.1:p.Ile383=
NM_000044.6:c.2745C>A MANE Select	NP_000035.2:p.Ile915=