Canonical Allele Identifier: CA2435119865

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686063C= , CM000685.2:g.67686063C=	GRCh38
NC_000023.10:g.66905905C= , CM000685.1:g.66905905C=	GRCh37
NC_000023.9:g.66822630C=	NCBI36
NG_009014.2:g.147032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*170C=	ENSP00000379358.4:n.*170C=
ENST00000374690.9:c.1822C= MANE Select	ENSP00000363822.3:p.Arg608=
ENST00000396043.3:c.449C=	ENSP00000379358.3:n.449C=
ENST00000396044.8:c.1822C=	ENSP00000379359.3:p.Arg608=
ENST00000612452.5:c.1822C=	ENSP00000484033.2:p.Arg608=
ENST00000374690.7:c.1822C=	ENSP00000363822.3:p.Arg608=
ENST00000396043.2:c.226C=	ENSP00000379358.2:p.Arg76=
ENST00000396044.7:c.1822C=	ENSP00000379359.3:p.Arg608=
ENST00000504326.5:c.1822C=	ENSP00000421155.1:p.Arg608=
ENST00000513847.5:n.2149C=
ENST00000514029.5:c.*303C=	ENSP00000425199.1:n.*303C=
ENST00000612010.4:c.*174C=	ENSP00000482407.1:n.*174C=
ENST00000612452.4:c.1252C=	ENSP00000484033.1:p.Arg418=
ENST00000613054.2:c.*20C=	ENSP00000479013.1:n.*20C=
NM_000044.3:c.1822C=	NP_000035.2:p.Arg608=
NM_001011645.2:c.226C=	NP_001011645.1:p.Arg76=
NM_000044.4:c.1822C=	NP_000035.2:p.Arg608=
NM_001011645.3:c.226C=	NP_001011645.1:p.Arg76=
NM_001348061.1:c.1822C=	NP_001334990.1:p.Arg608=
NM_001348063.1:c.1822C=	NP_001334992.1:p.Arg608=
NM_001348064.1:c.*20C=	NP_001334993.1:n.*20C=
NM_000044.6:c.1822C= MANE Select	NP_000035.2:p.Arg608=