Canonical Allele Identifier: CA413427695

Gene: AR

Linked Data

• dbSNP Id: rs1202166699
• gnomAD v2: X-66942710-C-G
• gnomAD v4: X-67722868-C-G
• MyVariant Identifiers: chrX:g.66942710C>G (hg19) ; chrX:g.67722868C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67722868C>G , CM000685.2:g.67722868C>G	GRCh38
NC_000023.10:g.66942710C>G , CM000685.1:g.66942710C>G	GRCh37
NC_000023.9:g.66859435C>G	NCBI36
NG_009014.2:g.183837C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*839C>G	ENSP00000379358.4:n.*839C>G
ENST00000374690.9:c.2491C>G MANE Select	ENSP00000363822.3:p.Leu831Val
ENST00000396043.3:c.1118C>G	ENSP00000379358.3:n.1118C>G
ENST00000396044.8:c.2174-818C>G	ENSP00000379359.3:n.2174-818C>G
ENST00000612452.5:c.2491C>G	ENSP00000484033.2:p.Leu831Val
ENST00000374690.7:c.2491C>G	ENSP00000363822.3:p.Leu831Val
ENST00000396043.2:c.895C>G	ENSP00000379358.2:p.Leu299Val
ENST00000396044.7:c.2174-818C>G	ENSP00000379359.3:n.2174-818C>G
ENST00000612452.4:c.1942C>G	ENSP00000484033.1:p.Leu648Val
NM_000044.3:c.2491C>G	NP_000035.2:p.Leu831Val
NM_001011645.2:c.895C>G	NP_001011645.1:p.Leu299Val
NM_000044.4:c.2491C>G	NP_000035.2:p.Leu831Val
NM_001011645.3:c.895C>G	NP_001011645.1:p.Leu299Val
NM_000044.6:c.2491C>G MANE Select	NP_000035.2:p.Leu831Val