Canonical Allele Identifier: CA2435134847

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722944G= , CM000685.2:g.67722944G=	GRCh38
NC_000023.10:g.66942786G= , CM000685.1:g.66942786G=	GRCh37
NC_000023.9:g.66859511G=	NCBI36
NG_009014.2:g.183913G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2567G= MANE Select	NP_000035.2:p.Arg856=
ENST00000374690.9:c.2567G= MANE Select	ENSP00000363822.3:p.Arg856=
NM_000044.3:c.2567G=	NP_000035.2:p.Arg856=
NM_000044.4:c.2567G=	NP_000035.2:p.Arg856=
NM_001011645.2:c.971G=	NP_001011645.1:p.Arg324=
NM_001011645.3:c.971G=	NP_001011645.1:p.Arg324=
ENST00000374690.7:c.2567G=	ENSP00000363822.3:p.Arg856=
ENST00000396043.2:c.971G=	ENSP00000379358.2:p.Arg324=
ENST00000396043.3:c.1194G=	ENSP00000379358.3:n.1194G=
ENST00000396043.4:c.*915G=	ENSP00000379358.4:n.*915G=
ENST00000396044.7:c.2174-742G=	ENSP00000379359.3:n.2174-742G=
ENST00000396044.8:c.2174-742G=	ENSP00000379359.3:n.2174-742G=
ENST00000612452.4:c.2018G=	ENSP00000484033.1:p.Arg673=
ENST00000612452.5:c.2567G=	ENSP00000484033.2:p.Arg856=