Canonical Allele Identifier: CA413428240

Gene: AR

Linked Data

• dbSNP Id: rs2147540339
• MyVariant Identifiers: chrX:g.66943569C>G (hg19) ; chrX:g.67723727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723727C>G , CM000685.2:g.67723727C>G	GRCh38
NC_000023.10:g.66943569C>G , CM000685.1:g.66943569C>G	GRCh37
NC_000023.9:g.66860294C>G	NCBI36
NG_009014.2:g.184696C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*997C>G	ENSP00000379358.4:n.*997C>G
ENST00000374690.9:c.2649C>G MANE Select	ENSP00000363822.3:p.Ile883Met
ENST00000396043.3:c.1276C>G	ENSP00000379358.3:n.1276C>G
ENST00000396044.8:c.*10C>G	ENSP00000379359.3:n.*10C>G
ENST00000612452.5:c.2649C>G	ENSP00000484033.2:p.Ile883Met
ENST00000374690.7:c.2649C>G	ENSP00000363822.3:p.Ile883Met
ENST00000396043.2:c.1053C>G	ENSP00000379358.2:p.Ile351Met
ENST00000396044.7:c.*10C>G	ENSP00000379359.3:n.*10C>G
ENST00000612452.4:c.2100C>G	ENSP00000484033.1:p.Ile700Met
NM_000044.3:c.2649C>G	NP_000035.2:p.Ile883Met
NM_001011645.2:c.1053C>G	NP_001011645.1:p.Ile351Met
NM_000044.4:c.2649C>G	NP_000035.2:p.Ile883Met
NM_001011645.3:c.1053C>G	NP_001011645.1:p.Ile351Met
NM_000044.6:c.2649C>G MANE Select	NP_000035.2:p.Ile883Met