Canonical Allele Identifier: CA413426617

Gene: AR

Linked Data

• MyVariant Identifiers: chrX:g.66941722G>A (hg19) ; chrX:g.67721880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721880G>A , CM000685.2:g.67721880G>A	GRCh38
NC_000023.10:g.66941722G>A , CM000685.1:g.66941722G>A	GRCh37
NC_000023.9:g.66858447G>A	NCBI36
NG_009014.2:g.182849G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*714G>A	ENSP00000379358.4:n.*714G>A
ENST00000374690.9:c.2366G>A MANE Select	ENSP00000363822.3:p.Arg789Lys
ENST00000396043.3:c.993G>A	ENSP00000379358.3:n.993G>A
ENST00000396044.8:c.2174-1806G>A	ENSP00000379359.3:n.2174-1806G>A
ENST00000612452.5:c.2366G>A	ENSP00000484033.2:p.Arg789Lys
ENST00000374690.7:c.2366G>A	ENSP00000363822.3:p.Arg789Lys
ENST00000396043.2:c.770G>A	ENSP00000379358.2:p.Arg257Lys
ENST00000396044.7:c.2174-1806G>A	ENSP00000379359.3:n.2174-1806G>A
ENST00000612452.4:c.1796G>A	ENSP00000484033.1:p.Arg599Lys
NM_000044.3:c.2366G>A	NP_000035.2:p.Arg789Lys
NM_001011645.2:c.770G>A	NP_001011645.1:p.Arg257Lys
NM_000044.4:c.2366G>A	NP_000035.2:p.Arg789Lys
NM_001011645.3:c.770G>A	NP_001011645.1:p.Arg257Lys
NM_000044.6:c.2366G>A MANE Select	NP_000035.2:p.Arg789Lys