Canonical Allele Identifier: CA2435132669

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717608T= , CM000685.2:g.67717608T=	GRCh38
NC_000023.10:g.66937450T= , CM000685.1:g.66937450T=	GRCh37
NC_000023.9:g.66854175T=	NCBI36
NG_009014.2:g.178577T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*652T=	ENSP00000379358.4:n.*652T=
ENST00000374690.9:c.2304T= MANE Select	ENSP00000363822.3:p.Asp768=
ENST00000396043.3:c.931T=	ENSP00000379358.3:n.931T=
ENST00000396044.8:c.2173+5919T=	ENSP00000379359.3:n.2173+5919T=
ENST00000612452.5:c.2304T=	ENSP00000484033.2:p.Asp768=
ENST00000374690.7:c.2304T=	ENSP00000363822.3:p.Asp768=
ENST00000396043.2:c.708T=	ENSP00000379358.2:p.Asp236=
ENST00000396044.7:c.2173+5919T=	ENSP00000379359.3:n.2173+5919T=
ENST00000612452.4:c.1734T=	ENSP00000484033.1:p.Asp578=
NM_000044.3:c.2304T=	NP_000035.2:p.Asp768=
NM_001011645.2:c.708T=	NP_001011645.1:p.Asp236=
NM_000044.4:c.2304T=	NP_000035.2:p.Asp768=
NM_001011645.3:c.708T=	NP_001011645.1:p.Asp236=
NM_000044.6:c.2304T= MANE Select	NP_000035.2:p.Asp768=