Canonical Allele Identifier: CA2435134324

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721837C= , CM000685.2:g.67721837C=	GRCh38
NC_000023.10:g.66941679C= , CM000685.1:g.66941679C=	GRCh37
NC_000023.9:g.66858404C=	NCBI36
NG_009014.2:g.182806C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*671C=	ENSP00000379358.4:n.*671C=
ENST00000374690.9:c.2323C= MANE Select	ENSP00000363822.3:p.Arg775=
ENST00000396043.3:c.950C=	ENSP00000379358.3:n.950C=
ENST00000396044.8:c.2174-1849C=	ENSP00000379359.3:n.2174-1849C=
ENST00000612452.5:c.2323C=	ENSP00000484033.2:p.Arg775=
ENST00000374690.7:c.2323C=	ENSP00000363822.3:p.Arg775=
ENST00000396043.2:c.727C=	ENSP00000379358.2:p.Arg243=
ENST00000396044.7:c.2174-1849C=	ENSP00000379359.3:n.2174-1849C=
ENST00000612452.4:c.1753C=	ENSP00000484033.1:p.Arg585=
NM_000044.3:c.2323C=	NP_000035.2:p.Arg775=
NM_001011645.2:c.727C=	NP_001011645.1:p.Arg243=
NM_000044.4:c.2323C=	NP_000035.2:p.Arg775=
NM_001011645.3:c.727C=	NP_001011645.1:p.Arg243=
NM_000044.6:c.2323C= MANE Select	NP_000035.2:p.Arg775=