Canonical Allele Identifier: CA2435134334

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721857G= , CM000685.2:g.67721857G=	GRCh38
NC_000023.10:g.66941699G= , CM000685.1:g.66941699G=	GRCh37
NC_000023.9:g.66858424G=	NCBI36
NG_009014.2:g.182826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*691G=	ENSP00000379358.4:n.*691G=
ENST00000374690.9:c.2343G= MANE Select	ENSP00000363822.3:p.Met781=
ENST00000396043.3:c.970G=	ENSP00000379358.3:n.970G=
ENST00000396044.8:c.2174-1829G=	ENSP00000379359.3:n.2174-1829G=
ENST00000612452.5:c.2343G=	ENSP00000484033.2:p.Met781=
ENST00000374690.7:c.2343G=	ENSP00000363822.3:p.Met781=
ENST00000396043.2:c.747G=	ENSP00000379358.2:p.Met249=
ENST00000396044.7:c.2174-1829G=	ENSP00000379359.3:n.2174-1829G=
ENST00000612452.4:c.1773G=	ENSP00000484033.1:p.Met591=
NM_000044.3:c.2343G=	NP_000035.2:p.Met781=
NM_001011645.2:c.747G=	NP_001011645.1:p.Met249=
NM_000044.4:c.2343G=	NP_000035.2:p.Met781=
NM_001011645.3:c.747G=	NP_001011645.1:p.Met249=
NM_000044.6:c.2343G= MANE Select	NP_000035.2:p.Met781=