Canonical Allele Identifier: CA10436590

Gene: AR

Linked Data

• dbSNP Id: rs371609746
• ExAC: X:66937276 G / A
• gnomAD v2: X-66937276-G-A
• gnomAD v3: X-67717434-G-A
• gnomAD v4: X-67717434-G-A
• MyVariant Identifiers: chrX:g.66937276G>A (hg19) ; chrX:g.67717434G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717434G>A , CM000685.2:g.67717434G>A	GRCh38
NC_000023.10:g.66937276G>A , CM000685.1:g.66937276G>A	GRCh37
NC_000023.9:g.66854001G>A	NCBI36
NG_009014.2:g.178403G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*522-44G>A	ENSP00000379358.4:n.*522-44G>A
ENST00000374690.9:c.2174-44G>A MANE Select	ENSP00000363822.3:n.2174-44G>A
ENST00000396043.3:c.801-44G>A	ENSP00000379358.3:n.801-44G>A
ENST00000396044.8:c.2173+5745G>A	ENSP00000379359.3:n.2173+5745G>A
ENST00000612452.5:c.2174-44G>A	ENSP00000484033.2:n.2174-44G>A
ENST00000374690.7:c.2174-44G>A	ENSP00000363822.3:n.2174-44G>A
ENST00000396043.2:c.578-44G>A	ENSP00000379358.2:n.578-44G>A
ENST00000396044.7:c.2173+5745G>A	ENSP00000379359.3:n.2173+5745G>A
ENST00000612452.4:c.1604-44G>A	ENSP00000484033.1:n.1604-44G>A
NM_000044.3:c.2174-44G>A	NP_000035.2:n.2174-44G>A
NM_001011645.2:c.578-44G>A	NP_001011645.1:n.578-44G>A
NM_000044.4:c.2174-44G>A	NP_000035.2:n.2174-44G>A
NM_001011645.3:c.578-44G>A	NP_001011645.1:n.578-44G>A
NM_000044.6:c.2174-44G>A MANE Select	NP_000035.2:n.2174-44G>A