Canonical Allele Identifier: CA413424766

Gene: AR

Linked Data

• ClinVar Variation Id: 492794
• ClinVar RCV Id: RCV000584020 ; RCV001269864
• dbSNP Id: rs1555996867
• MyVariant Identifiers: chrX:g.66937445C>G (hg19) ; chrX:g.67717603C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717603C>G , CM000685.2:g.67717603C>G	GRCh38
NC_000023.10:g.66937445C>G , CM000685.1:g.66937445C>G	GRCh37
NC_000023.9:g.66854170C>G	NCBI36
NG_009014.2:g.178572C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*647C>G	ENSP00000379358.4:n.*647C>G
ENST00000374690.9:c.2299C>G MANE Select	ENSP00000363822.3:p.Pro767Ala
ENST00000396043.3:c.926C>G	ENSP00000379358.3:n.926C>G
ENST00000396044.8:c.2173+5914C>G	ENSP00000379359.3:n.2173+5914C>G
ENST00000612452.5:c.2299C>G	ENSP00000484033.2:p.Pro767Ala
ENST00000374690.7:c.2299C>G	ENSP00000363822.3:p.Pro767Ala
ENST00000396043.2:c.703C>G	ENSP00000379358.2:p.Pro235Ala
ENST00000396044.7:c.2173+5914C>G	ENSP00000379359.3:n.2173+5914C>G
ENST00000612452.4:c.1729C>G	ENSP00000484033.1:p.Pro577Ala
NM_000044.3:c.2299C>G	NP_000035.2:p.Pro767Ala
NM_001011645.2:c.703C>G	NP_001011645.1:p.Pro235Ala
NM_000044.4:c.2299C>G	NP_000035.2:p.Pro767Ala
NM_001011645.3:c.703C>G	NP_001011645.1:p.Pro235Ala
NM_000044.6:c.2299C>G MANE Select	NP_000035.2:p.Pro767Ala