Canonical Allele Identifier: CA2435134835

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722908C= , CM000685.2:g.67722908C=	GRCh38
NC_000023.10:g.66942750C= , CM000685.1:g.66942750C=	GRCh37
NC_000023.9:g.66859475C=	NCBI36
NG_009014.2:g.183877C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*879C=	ENSP00000379358.4:n.*879C=
ENST00000374690.9:c.2531C= MANE Select	ENSP00000363822.3:p.Ala844=
ENST00000396043.3:c.1158C=	ENSP00000379358.3:n.1158C=
ENST00000396044.8:c.2174-778C=	ENSP00000379359.3:n.2174-778C=
ENST00000612452.5:c.2531C=	ENSP00000484033.2:p.Ala844=
ENST00000374690.7:c.2531C=	ENSP00000363822.3:p.Ala844=
ENST00000396043.2:c.935C=	ENSP00000379358.2:p.Ala312=
ENST00000396044.7:c.2174-778C=	ENSP00000379359.3:n.2174-778C=
ENST00000612452.4:c.1982C=	ENSP00000484033.1:p.Ala661=
NM_000044.3:c.2531C=	NP_000035.2:p.Ala844=
NM_001011645.2:c.935C=	NP_001011645.1:p.Ala312=
NM_000044.4:c.2531C=	NP_000035.2:p.Ala844=
NM_001011645.3:c.935C=	NP_001011645.1:p.Ala312=
NM_000044.6:c.2531C= MANE Select	NP_000035.2:p.Ala844=