Canonical Allele Identifier: CA413423050

Gene: AR

Linked Data

• ClinVar Variation Id: 1705712
• ClinVar RCV Id: RCV002284026
• dbSNP Id: rs2147524252
• MyVariant Identifiers: chrX:g.66931291G>T (hg19) ; chrX:g.67711449G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711449G>T , CM000685.2:g.67711449G>T	GRCh38
NC_000023.10:g.66931291G>T , CM000685.1:g.66931291G>T	GRCh37
NC_000023.9:g.66848016G>T	NCBI36
NG_009014.2:g.172418G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*281G>T	ENSP00000379358.4:n.*281G>T
ENST00000374690.9:c.1933G>T MANE Select	ENSP00000363822.3:p.Glu645Ter
ENST00000396043.3:c.560G>T	ENSP00000379358.3:n.560G>T
ENST00000396044.8:c.1933G>T	ENSP00000379359.3:p.Glu645Ter
ENST00000612452.5:c.1933G>T	ENSP00000484033.2:p.Glu645Ter
ENST00000374690.7:c.1933G>T	ENSP00000363822.3:p.Glu645Ter
ENST00000396043.2:c.337G>T	ENSP00000379358.2:p.Glu113Ter
ENST00000396044.7:c.1933G>T	ENSP00000379359.3:p.Glu645Ter
ENST00000612452.4:c.1363G>T	ENSP00000484033.1:p.Glu455Ter
NM_000044.3:c.1933G>T	NP_000035.2:p.Glu645Ter
NM_001011645.2:c.337G>T	NP_001011645.1:p.Glu113Ter
NM_000044.4:c.1933G>T	NP_000035.2:p.Glu645Ter
NM_001011645.3:c.337G>T	NP_001011645.1:p.Glu113Ter
NM_000044.6:c.1933G>T MANE Select	NP_000035.2:p.Glu645Ter