Canonical Allele Identifier: CA413424452

Gene: AR

Linked Data

• gnomAD v4: X-67717516-A-G
• MyVariant Identifiers: chrX:g.66937358A>G (hg19) ; chrX:g.67717516A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717516A>G , CM000685.2:g.67717516A>G	GRCh38
NC_000023.10:g.66937358A>G , CM000685.1:g.66937358A>G	GRCh37
NC_000023.9:g.66854083A>G	NCBI36
NG_009014.2:g.178485A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*560A>G	ENSP00000379358.4:n.*560A>G
ENST00000374690.9:c.2212A>G MANE Select	ENSP00000363822.3:p.Ile738Val
ENST00000396043.3:c.839A>G	ENSP00000379358.3:n.839A>G
ENST00000396044.8:c.2173+5827A>G	ENSP00000379359.3:n.2173+5827A>G
ENST00000612452.5:c.2212A>G	ENSP00000484033.2:p.Ile738Val
ENST00000374690.7:c.2212A>G	ENSP00000363822.3:p.Ile738Val
ENST00000396043.2:c.616A>G	ENSP00000379358.2:p.Ile206Val
ENST00000396044.7:c.2173+5827A>G	ENSP00000379359.3:n.2173+5827A>G
ENST00000612452.4:c.1642A>G	ENSP00000484033.1:p.Ile548Val
NM_000044.3:c.2212A>G	NP_000035.2:p.Ile738Val
NM_001011645.2:c.616A>G	NP_001011645.1:p.Ile206Val
NM_000044.4:c.2212A>G	NP_000035.2:p.Ile738Val
NM_001011645.3:c.616A>G	NP_001011645.1:p.Ile206Val
NM_000044.6:c.2212A>G MANE Select	NP_000035.2:p.Ile738Val