Canonical Allele Identifier: CA413426747

Gene: AR

Linked Data

• dbSNP Id: rs2147535830
• COSMIC: COSM1715077 ; COSM1715078
• MyVariant Identifiers: chrX:g.66941743G>A (hg19) ; chrX:g.67721901G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721901G>A , CM000685.2:g.67721901G>A	GRCh38
NC_000023.10:g.66941743G>A , CM000685.1:g.66941743G>A	GRCh37
NC_000023.9:g.66858468G>A	NCBI36
NG_009014.2:g.182870G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*735G>A	ENSP00000379358.4:n.*735G>A
ENST00000374690.9:c.2387G>A MANE Select	ENSP00000363822.3:p.Gly796Glu
ENST00000396043.3:c.1014G>A	ENSP00000379358.3:n.1014G>A
ENST00000396044.8:c.2174-1785G>A	ENSP00000379359.3:n.2174-1785G>A
ENST00000612452.5:c.2387G>A	ENSP00000484033.2:p.Gly796Glu
ENST00000374690.7:c.2387G>A	ENSP00000363822.3:p.Gly796Glu
ENST00000396043.2:c.791G>A	ENSP00000379358.2:p.Gly264Glu
ENST00000396044.7:c.2174-1785G>A	ENSP00000379359.3:n.2174-1785G>A
ENST00000612452.4:c.1817G>A	ENSP00000484033.1:p.Gly606Glu
NM_000044.3:c.2387G>A	NP_000035.2:p.Gly796Glu
NM_001011645.2:c.791G>A	NP_001011645.1:p.Gly264Glu
NM_000044.4:c.2387G>A	NP_000035.2:p.Gly796Glu
NM_001011645.3:c.791G>A	NP_001011645.1:p.Gly264Glu
NM_000044.6:c.2387G>A MANE Select	NP_000035.2:p.Gly796Glu