Canonical Allele Identifier: CA2435134333

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721856T= , CM000685.2:g.67721856T=	GRCh38
NC_000023.10:g.66941698T= , CM000685.1:g.66941698T=	GRCh37
NC_000023.9:g.66858423T=	NCBI36
NG_009014.2:g.182825T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*690T=	ENSP00000379358.4:n.*690T=
ENST00000374690.9:c.2342T= MANE Select	ENSP00000363822.3:p.Met781=
ENST00000396043.3:c.969T=	ENSP00000379358.3:n.969T=
ENST00000396044.8:c.2174-1830T=	ENSP00000379359.3:n.2174-1830T=
ENST00000612452.5:c.2342T=	ENSP00000484033.2:p.Met781=
ENST00000374690.7:c.2342T=	ENSP00000363822.3:p.Met781=
ENST00000396043.2:c.746T=	ENSP00000379358.2:p.Met249=
ENST00000396044.7:c.2174-1830T=	ENSP00000379359.3:n.2174-1830T=
ENST00000612452.4:c.1772T=	ENSP00000484033.1:p.Met591=
NM_000044.3:c.2342T=	NP_000035.2:p.Met781=
NM_001011645.2:c.746T=	NP_001011645.1:p.Met249=
NM_000044.4:c.2342T=	NP_000035.2:p.Met781=
NM_001011645.3:c.746T=	NP_001011645.1:p.Met249=
NM_000044.6:c.2342T= MANE Select	NP_000035.2:p.Met781=