Canonical Allele Identifier: CA2435130494

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711585A= , CM000685.2:g.67711585A=	GRCh38
NC_000023.10:g.66931427A= , CM000685.1:g.66931427A=	GRCh37
NC_000023.9:g.66848152A=	NCBI36
NG_009014.2:g.172554A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*417A=	ENSP00000379358.4:n.*417A=
ENST00000374690.9:c.2069A= MANE Select	ENSP00000363822.3:p.His690=
ENST00000396043.3:c.696A=	ENSP00000379358.3:n.696A=
ENST00000396044.8:c.2069A=	ENSP00000379359.3:p.His690=
ENST00000612452.5:c.2069A=	ENSP00000484033.2:p.His690=
ENST00000374690.7:c.2069A=	ENSP00000363822.3:p.His690=
ENST00000396043.2:c.473A=	ENSP00000379358.2:p.His158=
ENST00000396044.7:c.2069A=	ENSP00000379359.3:p.His690=
ENST00000612452.4:c.1499A=	ENSP00000484033.1:p.His500=
NM_000044.3:c.2069A=	NP_000035.2:p.His690=
NM_001011645.2:c.473A=	NP_001011645.1:p.His158=
NM_000044.4:c.2069A=	NP_000035.2:p.His690=
NM_001011645.3:c.473A=	NP_001011645.1:p.His158=
NM_000044.6:c.2069A= MANE Select	NP_000035.2:p.His690=