Canonical Allele Identifier: CA413428468

Gene: AR

Linked Data

• ClinVar Variation Id: 987520
• ClinVar RCV Id: RCV001268946
• dbSNP Id: rs2076147482
• MyVariant Identifiers: chrX:g.66943667A>C (hg19) ; chrX:g.67723825A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723825A>C , CM000685.2:g.67723825A>C	GRCh38
NC_000023.10:g.66943667A>C , CM000685.1:g.66943667A>C	GRCh37
NC_000023.9:g.66860392A>C	NCBI36
NG_009014.2:g.184794A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1095A>C	ENSP00000379358.4:n.*1095A>C
ENST00000374690.9:c.2747A>C MANE Select	ENSP00000363822.3:p.Tyr916Ser
ENST00000396043.3:c.1374A>C	ENSP00000379358.3:n.1374A>C
ENST00000396044.8:c.*108A>C	ENSP00000379359.3:n.*108A>C
ENST00000612452.5:c.2747A>C	ENSP00000484033.2:p.Tyr916Ser
ENST00000374690.7:c.2747A>C	ENSP00000363822.3:p.Tyr916Ser
ENST00000396043.2:c.1151A>C	ENSP00000379358.2:p.Tyr384Ser
ENST00000396044.7:c.*108A>C	ENSP00000379359.3:n.*108A>C
ENST00000612452.4:c.2198A>C	ENSP00000484033.1:p.Tyr733Ser
NM_000044.3:c.2747A>C	NP_000035.2:p.Tyr916Ser
NM_001011645.2:c.1151A>C	NP_001011645.1:p.Tyr384Ser
NM_000044.4:c.2747A>C	NP_000035.2:p.Tyr916Ser
NM_001011645.3:c.1151A>C	NP_001011645.1:p.Tyr384Ser
NM_000044.6:c.2747A>C MANE Select	NP_000035.2:p.Tyr916Ser