Canonical Allele Identifier: CA2435066105

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545227C= , CM000685.2:g.67545227C=	GRCh38
NC_000023.10:g.66765069C= , CM000685.1:g.66765069C=	GRCh37
NC_000023.9:g.66681794C=	NCBI36
NG_009014.2:g.6196C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.81C=	ENSP00000379358.4:p.Phe27=
ENST00000374690.9:c.81C= MANE Select	ENSP00000363822.3:p.Phe27=
ENST00000396044.8:c.81C=	ENSP00000379359.3:p.Phe27=
ENST00000612452.5:c.81C=	ENSP00000484033.2:p.Phe27=
ENST00000374690.7:c.81C=	ENSP00000363822.3:p.Phe27=
ENST00000396044.7:c.81C=	ENSP00000379359.3:p.Phe27=
ENST00000504326.5:c.81C=	ENSP00000421155.1:p.Phe27=
ENST00000513847.5:n.408C=
ENST00000514029.5:c.81C=	ENSP00000425199.1:p.Phe27=
ENST00000612010.4:c.81C=	ENSP00000482407.1:p.Phe27=
ENST00000612452.4:c.-490C=	ENSP00000484033.1:n.-490C=
ENST00000613054.2:c.81C=	ENSP00000479013.1:p.Phe27=
NM_000044.3:c.81C=	NP_000035.2:p.Phe27=
NM_000044.4:c.81C=	NP_000035.2:p.Phe27=
NM_001011645.3:c.-1703C=	NP_001011645.1:n.-1703C=
NM_001348061.1:c.81C=	NP_001334990.1:p.Phe27=
NM_001348063.1:c.81C=	NP_001334992.1:p.Phe27=
NM_001348064.1:c.81C=	NP_001334993.1:p.Phe27=
NM_000044.6:c.81C= MANE Select	NP_000035.2:p.Phe27=