Canonical Allele Identifier: CA2435130449

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711461A= , CM000685.2:g.67711461A=	GRCh38
NC_000023.10:g.66931303A= , CM000685.1:g.66931303A=	GRCh37
NC_000023.9:g.66848028A=	NCBI36
NG_009014.2:g.172430A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*293A=	ENSP00000379358.4:n.*293A=
ENST00000374690.9:c.1945A= MANE Select	ENSP00000363822.3:p.Thr649=
ENST00000396043.3:c.572A=	ENSP00000379358.3:n.572A=
ENST00000396044.8:c.1945A=	ENSP00000379359.3:p.Thr649=
ENST00000612452.5:c.1945A=	ENSP00000484033.2:p.Thr649=
ENST00000374690.7:c.1945A=	ENSP00000363822.3:p.Thr649=
ENST00000396043.2:c.349A=	ENSP00000379358.2:p.Thr117=
ENST00000396044.7:c.1945A=	ENSP00000379359.3:p.Thr649=
ENST00000612452.4:c.1375A=	ENSP00000484033.1:p.Thr459=
NM_000044.3:c.1945A=	NP_000035.2:p.Thr649=
NM_001011645.2:c.349A=	NP_001011645.1:p.Thr117=
NM_000044.4:c.1945A=	NP_000035.2:p.Thr649=
NM_001011645.3:c.349A=	NP_001011645.1:p.Thr117=
NM_000044.6:c.1945A= MANE Select	NP_000035.2:p.Thr649=