Canonical Allele Identifier: CA413424524

Gene: AR

Linked Data

• ClinVar Variation Id: 988510
• ClinVar RCV Id: RCV001269903
• dbSNP Id: rs2076118553
• MyVariant Identifiers: chrX:g.66937371G>C (hg19) ; chrX:g.67717529G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717529G>C , CM000685.2:g.67717529G>C	GRCh38
NC_000023.10:g.66937371G>C , CM000685.1:g.66937371G>C	GRCh37
NC_000023.9:g.66854096G>C	NCBI36
NG_009014.2:g.178498G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*573G>C	ENSP00000379358.4:n.*573G>C
ENST00000374690.9:c.2225G>C MANE Select	ENSP00000363822.3:p.Trp742Ser
ENST00000396043.3:c.852G>C	ENSP00000379358.3:n.852G>C
ENST00000396044.8:c.2173+5840G>C	ENSP00000379359.3:n.2173+5840G>C
ENST00000612452.5:c.2225G>C	ENSP00000484033.2:p.Trp742Ser
ENST00000374690.7:c.2225G>C	ENSP00000363822.3:p.Trp742Ser
ENST00000396043.2:c.629G>C	ENSP00000379358.2:p.Trp210Ser
ENST00000396044.7:c.2173+5840G>C	ENSP00000379359.3:n.2173+5840G>C
ENST00000612452.4:c.1655G>C	ENSP00000484033.1:p.Trp552Ser
NM_000044.3:c.2225G>C	NP_000035.2:p.Trp742Ser
NM_001011645.2:c.629G>C	NP_001011645.1:p.Trp210Ser
NM_000044.4:c.2225G>C	NP_000035.2:p.Trp742Ser
NM_001011645.3:c.629G>C	NP_001011645.1:p.Trp210Ser
NM_000044.6:c.2225G>C MANE Select	NP_000035.2:p.Trp742Ser