Canonical Allele Identifier: CA2435130503

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711604C= , CM000685.2:g.67711604C=	GRCh38
NC_000023.10:g.66931446C= , CM000685.1:g.66931446C=	GRCh37
NC_000023.9:g.66848171C=	NCBI36
NG_009014.2:g.172573C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*436C=	ENSP00000379358.4:n.*436C=
ENST00000374690.9:c.2088C= MANE Select	ENSP00000363822.3:p.Asp696=
ENST00000396043.3:c.715C=	ENSP00000379358.3:n.715C=
ENST00000396044.8:c.2088C=	ENSP00000379359.3:p.Asp696=
ENST00000612452.5:c.2088C=	ENSP00000484033.2:p.Asp696=
ENST00000374690.7:c.2088C=	ENSP00000363822.3:p.Asp696=
ENST00000396043.2:c.492C=	ENSP00000379358.2:p.Asp164=
ENST00000396044.7:c.2088C=	ENSP00000379359.3:p.Asp696=
ENST00000612452.4:c.1518C=	ENSP00000484033.1:p.Asp506=
NM_000044.3:c.2088C=	NP_000035.2:p.Asp696=
NM_001011645.2:c.492C=	NP_001011645.1:p.Asp164=
NM_000044.4:c.2088C=	NP_000035.2:p.Asp696=
NM_001011645.3:c.492C=	NP_001011645.1:p.Asp164=
NM_000044.6:c.2088C= MANE Select	NP_000035.2:p.Asp696=