Canonical Allele Identifier: CA413426539

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66941708G>T (hg19) ; chrX:g.67721866G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721866G>T , CM000685.2:g.67721866G>T	GRCh38
NC_000023.10:g.66941708G>T , CM000685.1:g.66941708G>T	GRCh37
NC_000023.9:g.66858433G>T	NCBI36
NG_009014.2:g.182835G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*700G>T	ENSP00000379358.4:n.*700G>T
ENST00000374690.9:c.2352G>T MANE Select	ENSP00000363822.3:p.Gln784His
ENST00000396043.3:c.979G>T	ENSP00000379358.3:n.979G>T
ENST00000396044.8:c.2174-1820G>T	ENSP00000379359.3:n.2174-1820G>T
ENST00000612452.5:c.2352G>T	ENSP00000484033.2:p.Gln784His
ENST00000374690.7:c.2352G>T	ENSP00000363822.3:p.Gln784His
ENST00000396043.2:c.756G>T	ENSP00000379358.2:p.Gln252His
ENST00000396044.7:c.2174-1820G>T	ENSP00000379359.3:n.2174-1820G>T
ENST00000612452.4:c.1782G>T	ENSP00000484033.1:p.Gln594His
NM_000044.3:c.2352G>T	NP_000035.2:p.Gln784His
NM_001011645.2:c.756G>T	NP_001011645.1:p.Gln252His
NM_000044.4:c.2352G>T	NP_000035.2:p.Gln784His
NM_001011645.3:c.756G>T	NP_001011645.1:p.Gln252His
NM_000044.6:c.2352G>T MANE Select	NP_000035.2:p.Gln784His