Canonical Allele Identifier: CA2435135172

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723818C= , CM000685.2:g.67723818C=	GRCh38
NC_000023.10:g.66943660C= , CM000685.1:g.66943660C=	GRCh37
NC_000023.9:g.66860385C=	NCBI36
NG_009014.2:g.184787C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1088C=	ENSP00000379358.4:n.*1088C=
ENST00000374690.9:c.2740C= MANE Select	ENSP00000363822.3:p.Pro914=
ENST00000396043.3:c.1367C=	ENSP00000379358.3:n.1367C=
ENST00000396044.8:c.*101C=	ENSP00000379359.3:n.*101C=
ENST00000612452.5:c.2740C=	ENSP00000484033.2:p.Pro914=
ENST00000374690.7:c.2740C=	ENSP00000363822.3:p.Pro914=
ENST00000396043.2:c.1144C=	ENSP00000379358.2:p.Pro382=
ENST00000396044.7:c.*101C=	ENSP00000379359.3:n.*101C=
ENST00000612452.4:c.2191C=	ENSP00000484033.1:p.Pro731=
NM_000044.3:c.2740C=	NP_000035.2:p.Pro914=
NM_001011645.2:c.1144C=	NP_001011645.1:p.Pro382=
NM_000044.4:c.2740C=	NP_000035.2:p.Pro914=
NM_001011645.3:c.1144C=	NP_001011645.1:p.Pro382=
NM_000044.6:c.2740C= MANE Select	NP_000035.2:p.Pro914=