Canonical Allele Identifier: CA413424529

Gene: AR

Linked Data

• COSMIC: COSM5572266 ; COSM5572267 ; COSM5572268
• MyVariant Identifiers: chrX:g.66937372G>T (hg19) ; chrX:g.67717530G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67717530G>T , CM000685.2:g.67717530G>T	GRCh38
NC_000023.10:g.66937372G>T , CM000685.1:g.66937372G>T	GRCh37
NC_000023.9:g.66854097G>T	NCBI36
NG_009014.2:g.178499G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*574G>T	ENSP00000379358.4:n.*574G>T
ENST00000374690.9:c.2226G>T MANE Select	ENSP00000363822.3:p.Trp742Cys
ENST00000396043.3:c.853G>T	ENSP00000379358.3:n.853G>T
ENST00000396044.8:c.2173+5841G>T	ENSP00000379359.3:n.2173+5841G>T
ENST00000612452.5:c.2226G>T	ENSP00000484033.2:p.Trp742Cys
ENST00000374690.7:c.2226G>T	ENSP00000363822.3:p.Trp742Cys
ENST00000396043.2:c.630G>T	ENSP00000379358.2:p.Trp210Cys
ENST00000396044.7:c.2173+5841G>T	ENSP00000379359.3:n.2173+5841G>T
ENST00000612452.4:c.1656G>T	ENSP00000484033.1:p.Trp552Cys
NM_000044.3:c.2226G>T	NP_000035.2:p.Trp742Cys
NM_001011645.2:c.630G>T	NP_001011645.1:p.Trp210Cys
NM_000044.4:c.2226G>T	NP_000035.2:p.Trp742Cys
NM_001011645.3:c.630G>T	NP_001011645.1:p.Trp210Cys
NM_000044.6:c.2226G>T MANE Select	NP_000035.2:p.Trp742Cys