Canonical Allele Identifier: CA413428471

Gene: AR

Linked Data

• dbSNP Id: rs2147540833
• MyVariant Identifiers: chrX:g.66943668T>A (hg19) ; chrX:g.67723826T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723826T>A , CM000685.2:g.67723826T>A	GRCh38
NC_000023.10:g.66943668T>A , CM000685.1:g.66943668T>A	GRCh37
NC_000023.9:g.66860393T>A	NCBI36
NG_009014.2:g.184795T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*1096T>A	ENSP00000379358.4:n.*1096T>A
ENST00000374690.9:c.2748T>A MANE Select	ENSP00000363822.3:p.Tyr916Ter
ENST00000396043.3:c.1375T>A	ENSP00000379358.3:n.1375T>A
ENST00000396044.8:c.*109T>A	ENSP00000379359.3:n.*109T>A
ENST00000612452.5:c.2748T>A	ENSP00000484033.2:p.Tyr916Ter
ENST00000374690.7:c.2748T>A	ENSP00000363822.3:p.Tyr916Ter
ENST00000396043.2:c.1152T>A	ENSP00000379358.2:p.Tyr384Ter
ENST00000396044.7:c.*109T>A	ENSP00000379359.3:n.*109T>A
ENST00000612452.4:c.2199T>A	ENSP00000484033.1:p.Tyr733Ter
NM_000044.3:c.2748T>A	NP_000035.2:p.Tyr916Ter
NM_001011645.2:c.1152T>A	NP_001011645.1:p.Tyr384Ter
NM_000044.4:c.2748T>A	NP_000035.2:p.Tyr916Ter
NM_001011645.3:c.1152T>A	NP_001011645.1:p.Tyr384Ter
NM_000044.6:c.2748T>A MANE Select	NP_000035.2:p.Tyr916Ter