Canonical Allele Identifier: CA2435132645

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717536G= , CM000685.2:g.67717536G=	GRCh38
NC_000023.10:g.66937378G= , CM000685.1:g.66937378G=	GRCh37
NC_000023.9:g.66854103G=	NCBI36
NG_009014.2:g.178505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*580G=	ENSP00000379358.4:n.*580G=
ENST00000374690.9:c.2232G= MANE Select	ENSP00000363822.3:p.Gly744=
ENST00000396043.3:c.859G=	ENSP00000379358.3:n.859G=
ENST00000396044.8:c.2173+5847G=	ENSP00000379359.3:n.2173+5847G=
ENST00000612452.5:c.2232G=	ENSP00000484033.2:p.Gly744=
ENST00000374690.7:c.2232G=	ENSP00000363822.3:p.Gly744=
ENST00000396043.2:c.636G=	ENSP00000379358.2:p.Gly212=
ENST00000396044.7:c.2173+5847G=	ENSP00000379359.3:n.2173+5847G=
ENST00000612452.4:c.1662G=	ENSP00000484033.1:p.Gly554=
NM_000044.3:c.2232G=	NP_000035.2:p.Gly744=
NM_001011645.2:c.636G=	NP_001011645.1:p.Gly212=
NM_000044.4:c.2232G=	NP_000035.2:p.Gly744=
NM_001011645.3:c.636G=	NP_001011645.1:p.Gly212=
NM_000044.6:c.2232G= MANE Select	NP_000035.2:p.Gly744=