Canonical Allele Identifier: CA413427658

Gene: AR

Linked Data

• ClinVar Variation Id: 1686658
• ClinVar RCV Id: RCV002331856
• dbSNP Id: rs2147537798
• MyVariant Identifiers: chrX:g.66942703T>A (hg19) ; chrX:g.67722861T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722861T>A , CM000685.2:g.67722861T>A	GRCh38
NC_000023.10:g.66942703T>A , CM000685.1:g.66942703T>A	GRCh37
NC_000023.9:g.66859428T>A	NCBI36
NG_009014.2:g.183830T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*832T>A	ENSP00000379358.4:n.*832T>A
ENST00000374690.9:c.2484T>A MANE Select	ENSP00000363822.3:p.Phe828Leu
ENST00000396043.3:c.1111T>A	ENSP00000379358.3:n.1111T>A
ENST00000396044.8:c.2174-825T>A	ENSP00000379359.3:n.2174-825T>A
ENST00000612452.5:c.2484T>A	ENSP00000484033.2:p.Phe828Leu
ENST00000374690.7:c.2484T>A	ENSP00000363822.3:p.Phe828Leu
ENST00000396043.2:c.888T>A	ENSP00000379358.2:p.Phe296Leu
ENST00000396044.7:c.2174-825T>A	ENSP00000379359.3:n.2174-825T>A
ENST00000612452.4:c.1935T>A	ENSP00000484033.1:p.Phe645Leu
NM_000044.3:c.2484T>A	NP_000035.2:p.Phe828Leu
NM_001011645.2:c.888T>A	NP_001011645.1:p.Phe296Leu
NM_000044.4:c.2484T>A	NP_000035.2:p.Phe828Leu
NM_001011645.3:c.888T>A	NP_001011645.1:p.Phe296Leu
NM_000044.6:c.2484T>A MANE Select	NP_000035.2:p.Phe828Leu