Canonical Allele Identifier: CA2435066092

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67545183C= , CM000685.2:g.67545183C=	GRCh38
NC_000023.10:g.66765025C= , CM000685.1:g.66765025C=	GRCh37
NC_000023.9:g.66681750C=	NCBI36
NG_009014.2:g.6152C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.37C=	ENSP00000379358.4:p.Arg13=
ENST00000374690.9:c.37C= MANE Select	ENSP00000363822.3:p.Arg13=
ENST00000396044.8:c.37C=	ENSP00000379359.3:p.Arg13=
ENST00000612452.5:c.37C=	ENSP00000484033.2:p.Arg13=
ENST00000374690.7:c.37C=	ENSP00000363822.3:p.Arg13=
ENST00000396044.7:c.37C=	ENSP00000379359.3:p.Arg13=
ENST00000504326.5:c.37C=	ENSP00000421155.1:p.Arg13=
ENST00000513847.5:n.364C=
ENST00000514029.5:c.37C=	ENSP00000425199.1:p.Arg13=
ENST00000612010.4:c.37C=	ENSP00000482407.1:p.Arg13=
ENST00000612452.4:c.-534C=	ENSP00000484033.1:n.-534C=
ENST00000613054.2:c.37C=	ENSP00000479013.1:p.Arg13=
NM_000044.3:c.37C=	NP_000035.2:p.Arg13=
NM_000044.4:c.37C=	NP_000035.2:p.Arg13=
NM_001011645.3:c.-1747C=	NP_001011645.1:n.-1747C=
NM_001348061.1:c.37C=	NP_001334990.1:p.Arg13=
NM_001348063.1:c.37C=	NP_001334992.1:p.Arg13=
NM_001348064.1:c.37C=	NP_001334993.1:p.Arg13=
NM_000044.6:c.37C= MANE Select	NP_000035.2:p.Arg13=