Canonical Allele Identifier: CA413426852

Gene: AR

Linked Data

• dbSNP Id: rs2147535902
• MyVariant Identifiers: chrX:g.66941760C>A (hg19) ; chrX:g.67721918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721918C>A , CM000685.2:g.67721918C>A	GRCh38
NC_000023.10:g.66941760C>A , CM000685.1:g.66941760C>A	GRCh37
NC_000023.9:g.66858485C>A	NCBI36
NG_009014.2:g.182887C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*752C>A	ENSP00000379358.4:n.*752C>A
ENST00000374690.9:c.2404C>A MANE Select	ENSP00000363822.3:p.Pro802Thr
ENST00000396043.3:c.1031C>A	ENSP00000379358.3:n.1031C>A
ENST00000396044.8:c.2174-1768C>A	ENSP00000379359.3:n.2174-1768C>A
ENST00000612452.5:c.2404C>A	ENSP00000484033.2:p.Pro802Thr
ENST00000374690.7:c.2404C>A	ENSP00000363822.3:p.Pro802Thr
ENST00000396043.2:c.808C>A	ENSP00000379358.2:p.Pro270Thr
ENST00000396044.7:c.2174-1768C>A	ENSP00000379359.3:n.2174-1768C>A
ENST00000612452.4:c.1834C>A	ENSP00000484033.1:p.Pro612Thr
NM_000044.3:c.2404C>A	NP_000035.2:p.Pro802Thr
NM_001011645.2:c.808C>A	NP_001011645.1:p.Pro270Thr
NM_000044.4:c.2404C>A	NP_000035.2:p.Pro802Thr
NM_001011645.3:c.808C>A	NP_001011645.1:p.Pro270Thr
NM_000044.6:c.2404C>A MANE Select	NP_000035.2:p.Pro802Thr