Canonical Allele Identifier: CA413428259

Gene: AR

Linked Data

• ClinVar Variation Id: 1202585
• ClinVar RCV Id: RCV001568310
• dbSNP Id: rs2147540378
• MyVariant Identifiers: chrX:g.66943577A>T (hg19) ; chrX:g.67723735A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723735A>T , CM000685.2:g.67723735A>T	GRCh38
NC_000023.10:g.66943577A>T , CM000685.1:g.66943577A>T	GRCh37
NC_000023.9:g.66860302A>T	NCBI36
NG_009014.2:g.184704A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1005A>T	ENSP00000379358.4:n.*1005A>T
ENST00000374690.9:c.2657A>T MANE Select	ENSP00000363822.3:p.His886Leu
ENST00000396043.3:c.1284A>T	ENSP00000379358.3:n.1284A>T
ENST00000396044.8:c.*18A>T	ENSP00000379359.3:n.*18A>T
ENST00000612452.5:c.2657A>T	ENSP00000484033.2:p.His886Leu
ENST00000374690.7:c.2657A>T	ENSP00000363822.3:p.His886Leu
ENST00000396043.2:c.1061A>T	ENSP00000379358.2:p.His354Leu
ENST00000396044.7:c.*18A>T	ENSP00000379359.3:n.*18A>T
ENST00000612452.4:c.2108A>T	ENSP00000484033.1:p.His703Leu
NM_000044.3:c.2657A>T	NP_000035.2:p.His886Leu
NM_001011645.2:c.1061A>T	NP_001011645.1:p.His354Leu
NM_000044.4:c.2657A>T	NP_000035.2:p.His886Leu
NM_001011645.3:c.1061A>T	NP_001011645.1:p.His354Leu
NM_000044.6:c.2657A>T MANE Select	NP_000035.2:p.His886Leu