Canonical Allele Identifier: CA2435134788

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723710A= , CM000685.2:g.67723710A=	GRCh38
NC_000023.10:g.66943552A= , CM000685.1:g.66943552A=	GRCh37
NC_000023.9:g.66860277A=	NCBI36
NG_009014.2:g.184679A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2632A= MANE Select	NP_000035.2:p.Thr878=
ENST00000374690.9:c.2632A= MANE Select	ENSP00000363822.3:p.Thr878=
NM_000044.3:c.2632A=	NP_000035.2:p.Thr878=
NM_000044.4:c.2632A=	NP_000035.2:p.Thr878=
NM_001011645.2:c.1036A=	NP_001011645.1:p.Thr346=
NM_001011645.3:c.1036A=	NP_001011645.1:p.Thr346=
ENST00000374690.7:c.2632A=	ENSP00000363822.3:p.Thr878=
ENST00000396043.2:c.1036A=	ENSP00000379358.2:p.Thr346=
ENST00000396043.3:c.1259A=	ENSP00000379358.3:n.1259A=
ENST00000396043.4:c.*980A=	ENSP00000379358.4:n.*980A=
ENST00000396044.7:c.2198A=	ENSP00000379359.3:p.His733=
ENST00000396044.8:c.2198A=	ENSP00000379359.3:p.His733=
ENST00000612452.4:c.2083A=	ENSP00000484033.1:p.Thr695=
ENST00000612452.5:c.2632A=	ENSP00000484033.2:p.Thr878=