Canonical Allele Identifier: CA2435134832

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722903C= , CM000685.2:g.67722903C=	GRCh38
NC_000023.10:g.66942745C= , CM000685.1:g.66942745C=	GRCh37
NC_000023.9:g.66859470C=	NCBI36
NG_009014.2:g.183872C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*874C=	ENSP00000379358.4:n.*874C=
ENST00000374690.9:c.2526C= MANE Select	ENSP00000363822.3:p.Ile842=
ENST00000396043.3:c.1153C=	ENSP00000379358.3:n.1153C=
ENST00000396044.8:c.2174-783C=	ENSP00000379359.3:n.2174-783C=
ENST00000612452.5:c.2526C=	ENSP00000484033.2:p.Ile842=
ENST00000374690.7:c.2526C=	ENSP00000363822.3:p.Ile842=
ENST00000396043.2:c.930C=	ENSP00000379358.2:p.Ile310=
ENST00000396044.7:c.2174-783C=	ENSP00000379359.3:n.2174-783C=
ENST00000612452.4:c.1977C=	ENSP00000484033.1:p.Ile659=
NM_000044.3:c.2526C=	NP_000035.2:p.Ile842=
NM_001011645.2:c.930C=	NP_001011645.1:p.Ile310=
NM_000044.4:c.2526C=	NP_000035.2:p.Ile842=
NM_001011645.3:c.930C=	NP_001011645.1:p.Ile310=
NM_000044.6:c.2526C= MANE Select	NP_000035.2:p.Ile842=