Canonical Allele Identifier: CA413427605

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66942696A>G (hg19) ; chrX:g.67722854A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722854A>G , CM000685.2:g.67722854A>G	GRCh38
NC_000023.10:g.66942696A>G , CM000685.1:g.66942696A>G	GRCh37
NC_000023.9:g.66859421A>G	NCBI36
NG_009014.2:g.183823A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*825A>G	ENSP00000379358.4:n.*825A>G
ENST00000374690.9:c.2477A>G MANE Select	ENSP00000363822.3:p.Lys826Arg
ENST00000396043.3:c.1104A>G	ENSP00000379358.3:n.1104A>G
ENST00000396044.8:c.2174-832A>G	ENSP00000379359.3:n.2174-832A>G
ENST00000612452.5:c.2477A>G	ENSP00000484033.2:p.Lys826Arg
ENST00000374690.7:c.2477A>G	ENSP00000363822.3:p.Lys826Arg
ENST00000396043.2:c.881A>G	ENSP00000379358.2:p.Lys294Arg
ENST00000396044.7:c.2174-832A>G	ENSP00000379359.3:n.2174-832A>G
ENST00000612452.4:c.1928A>G	ENSP00000484033.1:p.Lys643Arg
NM_000044.3:c.2477A>G	NP_000035.2:p.Lys826Arg
NM_001011645.2:c.881A>G	NP_001011645.1:p.Lys294Arg
NM_000044.4:c.2477A>G	NP_000035.2:p.Lys826Arg
NM_001011645.3:c.881A>G	NP_001011645.1:p.Lys294Arg
NM_000044.6:c.2477A>G MANE Select	NP_000035.2:p.Lys826Arg