Canonical Allele Identifier: CA2435132639

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717520A= , CM000685.2:g.67717520A=	GRCh38
NC_000023.10:g.66937362A= , CM000685.1:g.66937362A=	GRCh37
NC_000023.9:g.66854087A=	NCBI36
NG_009014.2:g.178489A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*564A=	ENSP00000379358.4:n.*564A=
ENST00000374690.9:c.2216A= MANE Select	ENSP00000363822.3:p.Gln739=
ENST00000396043.3:c.843A=	ENSP00000379358.3:n.843A=
ENST00000396044.8:c.2173+5831A=	ENSP00000379359.3:n.2173+5831A=
ENST00000612452.5:c.2216A=	ENSP00000484033.2:p.Gln739=
ENST00000374690.7:c.2216A=	ENSP00000363822.3:p.Gln739=
ENST00000396043.2:c.620A=	ENSP00000379358.2:p.Gln207=
ENST00000396044.7:c.2173+5831A=	ENSP00000379359.3:n.2173+5831A=
ENST00000612452.4:c.1646A=	ENSP00000484033.1:p.Gln549=
NM_000044.3:c.2216A=	NP_000035.2:p.Gln739=
NM_001011645.2:c.620A=	NP_001011645.1:p.Gln207=
NM_000044.4:c.2216A=	NP_000035.2:p.Gln739=
NM_001011645.3:c.620A=	NP_001011645.1:p.Gln207=
NM_000044.6:c.2216A= MANE Select	NP_000035.2:p.Gln739=