Canonical Allele Identifier: CA413427073

Gene: AR

Linked Data

• dbSNP Id: rs1555997626
• MyVariant Identifiers: chrX:g.66941794T>A (hg19) ; chrX:g.67721952T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721952T>A , CM000685.2:g.67721952T>A	GRCh38
NC_000023.10:g.66941794T>A , CM000685.1:g.66941794T>A	GRCh37
NC_000023.9:g.66858519T>A	NCBI36
NG_009014.2:g.182921T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*786T>A	ENSP00000379358.4:n.*786T>A
ENST00000374690.9:c.2438T>A MANE Select	ENSP00000363822.3:p.Leu813His
ENST00000396043.3:c.1065T>A	ENSP00000379358.3:n.1065T>A
ENST00000396044.8:c.2174-1734T>A	ENSP00000379359.3:n.2174-1734T>A
ENST00000612452.5:c.2438T>A	ENSP00000484033.2:p.Leu813His
ENST00000374690.7:c.2438T>A	ENSP00000363822.3:p.Leu813His
ENST00000396043.2:c.842T>A	ENSP00000379358.2:p.Leu281His
ENST00000396044.7:c.2174-1734T>A	ENSP00000379359.3:n.2174-1734T>A
ENST00000612452.4:c.1868T>A	ENSP00000484033.1:p.Leu623His
NM_000044.3:c.2438T>A	NP_000035.2:p.Leu813His
NM_001011645.2:c.842T>A	NP_001011645.1:p.Leu281His
NM_000044.4:c.2438T>A	NP_000035.2:p.Leu813His
NM_001011645.3:c.842T>A	NP_001011645.1:p.Leu281His
NM_000044.6:c.2438T>A MANE Select	NP_000035.2:p.Leu813His