Canonical Allele Identifier: CA2435119858

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686034G= , CM000685.2:g.67686034G=	GRCh38
NC_000023.10:g.66905876G= , CM000685.1:g.66905876G=	GRCh37
NC_000023.9:g.66822601G=	NCBI36
NG_009014.2:g.147003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*141G=	ENSP00000379358.4:n.*141G=
ENST00000374690.9:c.1793G= MANE Select	ENSP00000363822.3:p.Ser598=
ENST00000396043.3:c.420G=	ENSP00000379358.3:n.420G=
ENST00000396044.8:c.1793G=	ENSP00000379359.3:p.Ser598=
ENST00000612452.5:c.1793G=	ENSP00000484033.2:p.Ser598=
ENST00000374690.7:c.1793G=	ENSP00000363822.3:p.Ser598=
ENST00000396043.2:c.197G=	ENSP00000379358.2:p.Ser66=
ENST00000396044.7:c.1793G=	ENSP00000379359.3:p.Ser598=
ENST00000504326.5:c.1793G=	ENSP00000421155.1:p.Ser598=
ENST00000513847.5:n.2120G=
ENST00000514029.5:c.*274G=	ENSP00000425199.1:n.*274G=
ENST00000612010.4:c.*145G=	ENSP00000482407.1:n.*145G=
ENST00000612452.4:c.1223G=	ENSP00000484033.1:p.Ser408=
ENST00000613054.2:c.1710G=	ENSP00000479013.1:p.Gln570=
NM_000044.3:c.1793G=	NP_000035.2:p.Ser598=
NM_001011645.2:c.197G=	NP_001011645.1:p.Ser66=
NM_000044.4:c.1793G=	NP_000035.2:p.Ser598=
NM_001011645.3:c.197G=	NP_001011645.1:p.Ser66=
NM_001348061.1:c.1793G=	NP_001334990.1:p.Ser598=
NM_001348063.1:c.1793G=	NP_001334992.1:p.Ser598=
NM_001348064.1:c.1710G=	NP_001334993.1:p.Gln570=
NM_000044.6:c.1793G= MANE Select	NP_000035.2:p.Ser598=