Canonical Allele Identifier: CA2435134841

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722929C= , CM000685.2:g.67722929C=	GRCh38
NC_000023.10:g.66942771C= , CM000685.1:g.66942771C=	GRCh37
NC_000023.9:g.66859496C=	NCBI36
NG_009014.2:g.183898C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*900C=	ENSP00000379358.4:n.*900C=
ENST00000374690.9:c.2552C= MANE Select	ENSP00000363822.3:p.Thr851=
ENST00000396043.3:c.1179C=	ENSP00000379358.3:n.1179C=
ENST00000396044.8:c.2174-757C=	ENSP00000379359.3:n.2174-757C=
ENST00000612452.5:c.2552C=	ENSP00000484033.2:p.Thr851=
ENST00000374690.7:c.2552C=	ENSP00000363822.3:p.Thr851=
ENST00000396043.2:c.956C=	ENSP00000379358.2:p.Thr319=
ENST00000396044.7:c.2174-757C=	ENSP00000379359.3:n.2174-757C=
ENST00000612452.4:c.2003C=	ENSP00000484033.1:p.Thr668=
NM_000044.3:c.2552C=	NP_000035.2:p.Thr851=
NM_001011645.2:c.956C=	NP_001011645.1:p.Thr319=
NM_000044.4:c.2552C=	NP_000035.2:p.Thr851=
NM_001011645.3:c.956C=	NP_001011645.1:p.Thr319=
NM_000044.6:c.2552C= MANE Select	NP_000035.2:p.Thr851=