Canonical Allele Identifier: CA2435119885

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67686110A= , CM000685.2:g.67686110A=	GRCh38
NC_000023.10:g.66905952A= , CM000685.1:g.66905952A=	GRCh37
NC_000023.9:g.66822677A=	NCBI36
NG_009014.2:g.147079A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*217A=	ENSP00000379358.4:n.*217A=
ENST00000374690.9:c.1869A= MANE Select	ENSP00000363822.3:p.Ala623=
ENST00000396043.3:c.496A=	ENSP00000379358.3:n.496A=
ENST00000396044.8:c.1869A=	ENSP00000379359.3:p.Ala623=
ENST00000612452.5:c.1869A=	ENSP00000484033.2:p.Ala623=
ENST00000374690.7:c.1869A=	ENSP00000363822.3:p.Ala623=
ENST00000396043.2:c.273A=	ENSP00000379358.2:p.Ala91=
ENST00000396044.7:c.1869A=	ENSP00000379359.3:p.Ala623=
ENST00000504326.5:c.1869A=	ENSP00000421155.1:p.Ala623=
ENST00000513847.5:n.2196A=
ENST00000514029.5:c.*350A=	ENSP00000425199.1:n.*350A=
ENST00000612010.4:c.*221A=	ENSP00000482407.1:n.*221A=
ENST00000612452.4:c.1299A=	ENSP00000484033.1:p.Ala433=
ENST00000613054.2:c.*67A=	ENSP00000479013.1:n.*67A=
NM_000044.3:c.1869A=	NP_000035.2:p.Ala623=
NM_001011645.2:c.273A=	NP_001011645.1:p.Ala91=
NM_000044.4:c.1869A=	NP_000035.2:p.Ala623=
NM_001011645.3:c.273A=	NP_001011645.1:p.Ala91=
NM_001348061.1:c.1869A=	NP_001334990.1:p.Ala623=
NM_001348063.1:c.1869A=	NP_001334992.1:p.Ala623=
NM_001348064.1:c.*67A=	NP_001334993.1:n.*67A=
NM_000044.6:c.1869A= MANE Select	NP_000035.2:p.Ala623=