Canonical Allele Identifier: CA10436576

Gene: AR

Linked Data

• ClinVar Variation Id: 2935295
• ClinVar RCV Id: RCV003790949
• dbSNP Id: rs374874245
• ExAC: X:66931464 C / G
• gnomAD v2: X-66931464-C-G
• gnomAD v3: X-67711622-C-G
• gnomAD v4: X-67711622-C-G
• MyVariant Identifiers: chrX:g.66931464C>G (hg19) ; chrX:g.67711622C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711622C>G , CM000685.2:g.67711622C>G	GRCh38
NC_000023.10:g.66931464C>G , CM000685.1:g.66931464C>G	GRCh37
NC_000023.9:g.66848189C>G	NCBI36
NG_009014.2:g.172591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*454C>G	ENSP00000379358.4:n.*454C>G
ENST00000374690.9:c.2106C>G MANE Select	ENSP00000363822.3:p.Leu702=
ENST00000396043.3:c.733C>G	ENSP00000379358.3:n.733C>G
ENST00000396044.8:c.2106C>G	ENSP00000379359.3:p.Leu702=
ENST00000612452.5:c.2106C>G	ENSP00000484033.2:p.Leu702=
ENST00000374690.7:c.2106C>G	ENSP00000363822.3:p.Leu702=
ENST00000396043.2:c.510C>G	ENSP00000379358.2:p.Leu170=
ENST00000396044.7:c.2106C>G	ENSP00000379359.3:p.Leu702=
ENST00000612452.4:c.1536C>G	ENSP00000484033.1:p.Leu512=
NM_000044.3:c.2106C>G	NP_000035.2:p.Leu702=
NM_001011645.2:c.510C>G	NP_001011645.1:p.Leu170=
NM_000044.4:c.2106C>G	NP_000035.2:p.Leu702=
NM_001011645.3:c.510C>G	NP_001011645.1:p.Leu170=
NM_000044.6:c.2106C>G MANE Select	NP_000035.2:p.Leu702=