Canonical Allele Identifier: CA2435130430

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711404C= , CM000685.2:g.67711404C=	GRCh38
NC_000023.10:g.66931246C= , CM000685.1:g.66931246C=	GRCh37
NC_000023.9:g.66847971C=	NCBI36
NG_009014.2:g.172373C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.1888C= MANE Select	NP_000035.2:p.Arg630=
ENST00000374690.9:c.1888C= MANE Select	ENSP00000363822.3:p.Arg630=
NM_000044.3:c.1888C=	NP_000035.2:p.Arg630=
NM_000044.4:c.1888C=	NP_000035.2:p.Arg630=
NM_001011645.2:c.292C=	NP_001011645.1:p.Arg98=
NM_001011645.3:c.292C=	NP_001011645.1:p.Arg98=
ENST00000374690.7:c.1888C=	ENSP00000363822.3:p.Arg630=
ENST00000396043.2:c.292C=	ENSP00000379358.2:p.Arg98=
ENST00000396043.3:c.515C=	ENSP00000379358.3:n.515C=
ENST00000396043.4:c.*236C=	ENSP00000379358.4:n.*236C=
ENST00000396044.7:c.1888C=	ENSP00000379359.3:p.Arg630=
ENST00000396044.8:c.1888C=	ENSP00000379359.3:p.Arg630=
ENST00000612452.4:c.1318C=	ENSP00000484033.1:p.Arg440=
ENST00000612452.5:c.1888C=	ENSP00000484033.2:p.Arg630=