Canonical Allele Identifier: CA2435134833

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722904A= , CM000685.2:g.67722904A=	GRCh38
NC_000023.10:g.66942746A= , CM000685.1:g.66942746A=	GRCh37
NC_000023.9:g.66859471A=	NCBI36
NG_009014.2:g.183873A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*875A=	ENSP00000379358.4:n.*875A=
ENST00000374690.9:c.2527A= MANE Select	ENSP00000363822.3:p.Ile843=
ENST00000396043.3:c.1154A=	ENSP00000379358.3:n.1154A=
ENST00000396044.8:c.2174-782A=	ENSP00000379359.3:n.2174-782A=
ENST00000612452.5:c.2527A=	ENSP00000484033.2:p.Ile843=
ENST00000374690.7:c.2527A=	ENSP00000363822.3:p.Ile843=
ENST00000396043.2:c.931A=	ENSP00000379358.2:p.Ile311=
ENST00000396044.7:c.2174-782A=	ENSP00000379359.3:n.2174-782A=
ENST00000612452.4:c.1978A=	ENSP00000484033.1:p.Ile660=
NM_000044.3:c.2527A=	NP_000035.2:p.Ile843=
NM_001011645.2:c.931A=	NP_001011645.1:p.Ile311=
NM_000044.4:c.2527A=	NP_000035.2:p.Ile843=
NM_001011645.3:c.931A=	NP_001011645.1:p.Ile311=
NM_000044.6:c.2527A= MANE Select	NP_000035.2:p.Ile843=