Canonical Allele Identifier: CA2435134355

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721934G= , CM000685.2:g.67721934G=	GRCh38
NC_000023.10:g.66941776G= , CM000685.1:g.66941776G=	GRCh37
NC_000023.9:g.66858501G=	NCBI36
NG_009014.2:g.182903G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2420G= MANE Select	NP_000035.2:p.Cys807=
ENST00000374690.9:c.2420G= MANE Select	ENSP00000363822.3:p.Cys807=
NM_000044.3:c.2420G=	NP_000035.2:p.Cys807=
NM_000044.4:c.2420G=	NP_000035.2:p.Cys807=
NM_001011645.2:c.824G=	NP_001011645.1:p.Cys275=
NM_001011645.3:c.824G=	NP_001011645.1:p.Cys275=
ENST00000374690.7:c.2420G=	ENSP00000363822.3:p.Cys807=
ENST00000396043.2:c.824G=	ENSP00000379358.2:p.Cys275=
ENST00000396043.3:c.1047G=	ENSP00000379358.3:n.1047G=
ENST00000396043.4:c.*768G=	ENSP00000379358.4:n.*768G=
ENST00000396044.7:c.2174-1752G=	ENSP00000379359.3:n.2174-1752G=
ENST00000396044.8:c.2174-1752G=	ENSP00000379359.3:n.2174-1752G=
ENST00000612452.4:c.1850G=	ENSP00000484033.1:p.Cys617=
ENST00000612452.5:c.2420G=	ENSP00000484033.2:p.Cys807=