Canonical Allele Identifier: CA10436554

Gene: AR

Linked Data

• ClinVar Variation Id: 2949312
• ClinVar RCV Id: RCV003802038
• dbSNP Id: rs375891414
• ExAC: X:66931240 A / G
• gnomAD v2: X-66931240-A-G
• gnomAD v3: X-67711398-A-G
• gnomAD v4: X-67711398-A-G
• MyVariant Identifiers: chrX:g.66931240A>G (hg19) ; chrX:g.67711398A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711398A>G , CM000685.2:g.67711398A>G	GRCh38
NC_000023.10:g.66931240A>G , CM000685.1:g.66931240A>G	GRCh37
NC_000023.9:g.66847965A>G	NCBI36
NG_009014.2:g.172367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*234-4A>G	ENSP00000379358.4:n.*234-4A>G
ENST00000374690.9:c.1886-4A>G MANE Select	ENSP00000363822.3:n.1886-4A>G
ENST00000396043.3:c.513-4A>G	ENSP00000379358.3:n.513-4A>G
ENST00000396044.8:c.1886-4A>G	ENSP00000379359.3:n.1886-4A>G
ENST00000612452.5:c.1886-4A>G	ENSP00000484033.2:n.1886-4A>G
ENST00000374690.7:c.1886-4A>G	ENSP00000363822.3:n.1886-4A>G
ENST00000396043.2:c.290-4A>G	ENSP00000379358.2:n.290-4A>G
ENST00000396044.7:c.1886-4A>G	ENSP00000379359.3:n.1886-4A>G
ENST00000612452.4:c.1316-4A>G	ENSP00000484033.1:n.1316-4A>G
NM_000044.3:c.1886-4A>G	NP_000035.2:n.1886-4A>G
NM_001011645.2:c.290-4A>G	NP_001011645.1:n.290-4A>G
NM_000044.4:c.1886-4A>G	NP_000035.2:n.1886-4A>G
NM_001011645.3:c.290-4A>G	NP_001011645.1:n.290-4A>G
NM_000044.6:c.1886-4A>G MANE Select	NP_000035.2:n.1886-4A>G