Canonical Allele Identifier: CA2435134814

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67723738_67723739delinsTG , CM000685.2:g.67723738_67723739delinsTG	GRCh38
NC_000023.10:g.66943580_66943581delinsTG , CM000685.1:g.66943580_66943581delinsTG	GRCh37
NC_000023.9:g.66860305_66860306delinsTG	NCBI36
NG_009014.2:g.184707_184708delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000396043.4:c.*1008_*1009delinsTG	ENSP00000379358.4:n.*1008_*1009delinsTG
ENST00000374690.9:c.2660_2661delinsTG MANE Select	ENSP00000363822.3:p.Met887=
ENST00000396043.3:c.1287_1288delinsTG	ENSP00000379358.3:n.1287_1288delinsTG
ENST00000396044.8:c.*21_*22delinsTG	ENSP00000379359.3:n.*21_*22delinsTG
ENST00000612452.5:c.2660_2661delinsTG	ENSP00000484033.2:p.Met887=
ENST00000374690.7:c.2660_2661delinsTG	ENSP00000363822.3:p.Met887=
ENST00000396043.2:c.1064_1065delinsTG	ENSP00000379358.2:p.Met355=
ENST00000396044.7:c.*21_*22delinsTG	ENSP00000379359.3:n.*21_*22delinsTG
ENST00000612452.4:c.2111_2112delinsTG	ENSP00000484033.1:p.Met704=
NM_000044.3:c.2660_2661delinsTG	NP_000035.2:p.Met887=
NM_001011645.2:c.1064_1065delinsTG	NP_001011645.1:p.Met355=
NM_000044.4:c.2660_2661delinsTG	NP_000035.2:p.Met887=
NM_001011645.3:c.1064_1065delinsTG	NP_001011645.1:p.Met355=
NM_000044.6:c.2660_2661delinsTG MANE Select	NP_000035.2:p.Met887=