Canonical Allele Identifier: CA2435130525

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711661C= , CM000685.2:g.67711661C=	GRCh38
NC_000023.10:g.66931503C= , CM000685.1:g.66931503C=	GRCh37
NC_000023.9:g.66848228C=	NCBI36
NG_009014.2:g.172630C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*493C=	ENSP00000379358.4:n.*493C=
ENST00000374690.9:c.2145C= MANE Select	ENSP00000363822.3:p.His715=
ENST00000396043.3:c.772C=	ENSP00000379358.3:n.772C=
ENST00000396044.8:c.2145C=	ENSP00000379359.3:p.His715=
ENST00000612452.5:c.2145C=	ENSP00000484033.2:p.His715=
ENST00000374690.7:c.2145C=	ENSP00000363822.3:p.His715=
ENST00000396043.2:c.549C=	ENSP00000379358.2:p.His183=
ENST00000396044.7:c.2145C=	ENSP00000379359.3:p.His715=
ENST00000612452.4:c.1575C=	ENSP00000484033.1:p.His525=
NM_000044.3:c.2145C=	NP_000035.2:p.His715=
NM_001011645.2:c.549C=	NP_001011645.1:p.His183=
NM_000044.4:c.2145C=	NP_000035.2:p.His715=
NM_001011645.3:c.549C=	NP_001011645.1:p.His183=
NM_000044.6:c.2145C= MANE Select	NP_000035.2:p.His715=