Canonical Allele Identifier: CA413427575

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722850C>A , CM000685.2:g.67722850C>A	GRCh38
NC_000023.10:g.66942692C>A , CM000685.1:g.66942692C>A	GRCh37
NC_000023.9:g.66859417C>A	NCBI36
NG_009014.2:g.183819C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000044.6:c.2473C>A MANE Select	NP_000035.2:p.Gln825Lys
ENST00000374690.9:c.2473C>A MANE Select	ENSP00000363822.3:p.Gln825Lys
NM_000044.3:c.2473C>A	NP_000035.2:p.Gln825Lys
NM_000044.4:c.2473C>A	NP_000035.2:p.Gln825Lys
NM_001011645.2:c.877C>A	NP_001011645.1:p.Gln293Lys
NM_001011645.3:c.877C>A	NP_001011645.1:p.Gln293Lys
ENST00000374690.7:c.2473C>A	ENSP00000363822.3:p.Gln825Lys
ENST00000396043.2:c.877C>A	ENSP00000379358.2:p.Gln293Lys
ENST00000396043.3:c.1100C>A	ENSP00000379358.3:n.1100C>A
ENST00000396043.4:c.*821C>A	ENSP00000379358.4:n.*821C>A
ENST00000396044.7:c.2174-836C>A	ENSP00000379359.3:n.2174-836C>A
ENST00000396044.8:c.2174-836C>A	ENSP00000379359.3:n.2174-836C>A
ENST00000612452.4:c.1924C>A	ENSP00000484033.1:p.Gln642Lys
ENST00000612452.5:c.2473C>A	ENSP00000484033.2:p.Gln825Lys