Canonical Allele Identifier: CA2435132598

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717431C= , CM000685.2:g.67717431C=	GRCh38
NC_000023.10:g.66937273C= , CM000685.1:g.66937273C=	GRCh37
NC_000023.9:g.66853998C=	NCBI36
NG_009014.2:g.178400C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522-47C=	ENSP00000379358.4:n.*522-47C=
ENST00000374690.9:c.2174-47C= MANE Select	ENSP00000363822.3:n.2174-47C=
ENST00000396043.3:c.801-47C=	ENSP00000379358.3:n.801-47C=
ENST00000396044.8:c.2173+5742C=	ENSP00000379359.3:n.2173+5742C=
ENST00000612452.5:c.2174-47C=	ENSP00000484033.2:n.2174-47C=
ENST00000374690.7:c.2174-47C=	ENSP00000363822.3:n.2174-47C=
ENST00000396043.2:c.578-47C=	ENSP00000379358.2:n.578-47C=
ENST00000396044.7:c.2173+5742C=	ENSP00000379359.3:n.2173+5742C=
ENST00000612452.4:c.1604-47C=	ENSP00000484033.1:n.1604-47C=
NM_000044.3:c.2174-47C=	NP_000035.2:n.2174-47C=
NM_001011645.2:c.578-47C=	NP_001011645.1:n.578-47C=
NM_000044.4:c.2174-47C=	NP_000035.2:n.2174-47C=
NM_001011645.3:c.578-47C=	NP_001011645.1:n.578-47C=
NM_000044.6:c.2174-47C= MANE Select	NP_000035.2:n.2174-47C=