Canonical Allele Identifier: CA3065189126

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711468G= , CM000685.2:g.67711468G=	GRCh38
NC_000023.10:g.66931310G= , CM000685.1:g.66931310G=	GRCh37
NC_000023.9:g.66848035G=	NCBI36
NG_009014.2:g.172437G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.1952G= MANE Select	NP_000035.2:p.Ser651=
ENST00000374690.9:c.1952G= MANE Select	ENSP00000363822.3:p.Ser651=
NM_000044.3:c.1952G=	NP_000035.2:p.Ser651=
NM_000044.4:c.1952G=	NP_000035.2:p.Ser651=
NM_001011645.2:c.356G=	NP_001011645.1:p.Ser119=
NM_001011645.3:c.356G=	NP_001011645.1:p.Ser119=
ENST00000374690.7:c.1952G=	ENSP00000363822.3:p.Ser651=
ENST00000396043.2:c.356G=	ENSP00000379358.2:p.Ser119=
ENST00000396043.3:c.579G=	ENSP00000379358.3:n.579G=
ENST00000396043.4:c.*300G=	ENSP00000379358.4:n.*300G=
ENST00000396044.7:c.1952G=	ENSP00000379359.3:p.Ser651=
ENST00000396044.8:c.1952G=	ENSP00000379359.3:p.Ser651=
ENST00000612452.4:c.1382G=	ENSP00000484033.1:p.Ser461=
ENST00000612452.5:c.1952G=	ENSP00000484033.2:p.Ser651=