Canonical Allele Identifier: CA2435119888

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686119T= , CM000685.2:g.67686119T=	GRCh38
NC_000023.10:g.66905961T= , CM000685.1:g.66905961T=	GRCh37
NC_000023.9:g.66822686T=	NCBI36
NG_009014.2:g.147088T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*226T=	ENSP00000379358.4:n.*226T=
ENST00000374690.9:c.1878T= MANE Select	ENSP00000363822.3:p.Thr626=
ENST00000396043.3:c.505T=	ENSP00000379358.3:n.505T=
ENST00000396044.8:c.1878T=	ENSP00000379359.3:p.Thr626=
ENST00000612452.5:c.1878T=	ENSP00000484033.2:p.Thr626=
ENST00000374690.7:c.1878T=	ENSP00000363822.3:p.Thr626=
ENST00000396043.2:c.282T=	ENSP00000379358.2:p.Thr94=
ENST00000396044.7:c.1878T=	ENSP00000379359.3:p.Thr626=
ENST00000504326.5:c.1878T=	ENSP00000421155.1:p.Thr626=
ENST00000513847.5:n.2205T=
ENST00000514029.5:c.*359T=	ENSP00000425199.1:n.*359T=
ENST00000612010.4:c.*230T=	ENSP00000482407.1:n.*230T=
ENST00000612452.4:c.1308T=	ENSP00000484033.1:p.Thr436=
ENST00000613054.2:c.*76T=	ENSP00000479013.1:n.*76T=
NM_000044.3:c.1878T=	NP_000035.2:p.Thr626=
NM_001011645.2:c.282T=	NP_001011645.1:p.Thr94=
NM_000044.4:c.1878T=	NP_000035.2:p.Thr626=
NM_001011645.3:c.282T=	NP_001011645.1:p.Thr94=
NM_001348061.1:c.1878T=	NP_001334990.1:p.Thr626=
NM_001348063.1:c.1878T=	NP_001334992.1:p.Thr626=
NM_001348064.1:c.*76T=	NP_001334993.1:n.*76T=
NM_000044.6:c.1878T= MANE Select	NP_000035.2:p.Thr626=