Canonical Allele Identifier: CA413426685

Gene: AR

Linked Data

• dbSNP Id: rs2076137520
• MyVariant Identifiers: chrX:g.66941733C>A (hg19) ; chrX:g.67721891C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67721891C>A , CM000685.2:g.67721891C>A	GRCh38
NC_000023.10:g.66941733C>A , CM000685.1:g.66941733C>A	GRCh37
NC_000023.9:g.66858458C>A	NCBI36
NG_009014.2:g.182860C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*725C>A	ENSP00000379358.4:n.*725C>A
ENST00000374690.9:c.2377C>A MANE Select	ENSP00000363822.3:p.Gln793Lys
ENST00000396043.3:c.1004C>A	ENSP00000379358.3:n.1004C>A
ENST00000396044.8:c.2174-1795C>A	ENSP00000379359.3:n.2174-1795C>A
ENST00000612452.5:c.2377C>A	ENSP00000484033.2:p.Gln793Lys
ENST00000374690.7:c.2377C>A	ENSP00000363822.3:p.Gln793Lys
ENST00000396043.2:c.781C>A	ENSP00000379358.2:p.Gln261Lys
ENST00000396044.7:c.2174-1795C>A	ENSP00000379359.3:n.2174-1795C>A
ENST00000612452.4:c.1807C>A	ENSP00000484033.1:p.Gln603Lys
NM_000044.3:c.2377C>A	NP_000035.2:p.Gln793Lys
NM_001011645.2:c.781C>A	NP_001011645.1:p.Gln261Lys
NM_000044.4:c.2377C>A	NP_000035.2:p.Gln793Lys
NM_001011645.3:c.781C>A	NP_001011645.1:p.Gln261Lys
NM_000044.6:c.2377C>A MANE Select	NP_000035.2:p.Gln793Lys