Canonical Allele Identifier: CA2435119875

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686088G= , CM000685.2:g.67686088G=	GRCh38
NC_000023.10:g.66905930G= , CM000685.1:g.66905930G=	GRCh37
NC_000023.9:g.66822655G=	NCBI36
NG_009014.2:g.147057G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*195G=	ENSP00000379358.4:n.*195G=
ENST00000374690.9:c.1847G= MANE Select	ENSP00000363822.3:p.Arg616=
ENST00000396043.3:c.474G=	ENSP00000379358.3:n.474G=
ENST00000396044.8:c.1847G=	ENSP00000379359.3:p.Arg616=
ENST00000612452.5:c.1847G=	ENSP00000484033.2:p.Arg616=
ENST00000374690.7:c.1847G=	ENSP00000363822.3:p.Arg616=
ENST00000396043.2:c.251G=	ENSP00000379358.2:p.Arg84=
ENST00000396044.7:c.1847G=	ENSP00000379359.3:p.Arg616=
ENST00000504326.5:c.1847G=	ENSP00000421155.1:p.Arg616=
ENST00000513847.5:n.2174G=
ENST00000514029.5:c.*328G=	ENSP00000425199.1:n.*328G=
ENST00000612010.4:c.*199G=	ENSP00000482407.1:n.*199G=
ENST00000612452.4:c.1277G=	ENSP00000484033.1:p.Arg426=
ENST00000613054.2:c.*45G=	ENSP00000479013.1:n.*45G=
NM_000044.3:c.1847G=	NP_000035.2:p.Arg616=
NM_001011645.2:c.251G=	NP_001011645.1:p.Arg84=
NM_000044.4:c.1847G=	NP_000035.2:p.Arg616=
NM_001011645.3:c.251G=	NP_001011645.1:p.Arg84=
NM_001348061.1:c.1847G=	NP_001334990.1:p.Arg616=
NM_001348063.1:c.1847G=	NP_001334992.1:p.Arg616=
NM_001348064.1:c.*45G=	NP_001334993.1:n.*45G=
NM_000044.6:c.1847G= MANE Select	NP_000035.2:p.Arg616=