Canonical Allele Identifier: CA2435132625

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717483C= , CM000685.2:g.67717483C=	GRCh38
NC_000023.10:g.66937325C= , CM000685.1:g.66937325C=	GRCh37
NC_000023.9:g.66854050C=	NCBI36
NG_009014.2:g.178452C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*527C=	ENSP00000379358.4:n.*527C=
ENST00000374690.9:c.2179C= MANE Select	ENSP00000363822.3:p.Arg727=
ENST00000396043.3:c.806C=	ENSP00000379358.3:n.806C=
ENST00000396044.8:c.2173+5794C=	ENSP00000379359.3:n.2173+5794C=
ENST00000612452.5:c.2179C=	ENSP00000484033.2:p.Arg727=
ENST00000374690.7:c.2179C=	ENSP00000363822.3:p.Arg727=
ENST00000396043.2:c.583C=	ENSP00000379358.2:p.Arg195=
ENST00000396044.7:c.2173+5794C=	ENSP00000379359.3:n.2173+5794C=
ENST00000612452.4:c.1609C=	ENSP00000484033.1:p.Arg537=
NM_000044.3:c.2179C=	NP_000035.2:p.Arg727=
NM_001011645.2:c.583C=	NP_001011645.1:p.Arg195=
NM_000044.4:c.2179C=	NP_000035.2:p.Arg727=
NM_001011645.3:c.583C=	NP_001011645.1:p.Arg195=
NM_000044.6:c.2179C= MANE Select	NP_000035.2:p.Arg727=