Canonical Allele Identifier: CA2435130531

Gene: AR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.67711674_67711675delinsGC , CM000685.2:g.67711674_67711675delinsGC	GRCh38
NC_000023.10:g.66931516_66931517delinsGC , CM000685.1:g.66931516_66931517delinsGC	GRCh37
NC_000023.9:g.66848241_66848242delinsGC	NCBI36
NG_009014.2:g.172643_172644delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396043.4:c.*506_*507delinsGC	ENSP00000379358.4:n.*506_*507delinsGC
ENST00000374690.9:c.2158_2159delinsGC MANE Select	ENSP00000363822.3:p.Ala720=
ENST00000396043.3:c.785_786delinsGC	ENSP00000379358.3:n.785_786delinsGC
ENST00000396044.8:c.2158_2159delinsGC	ENSP00000379359.3:p.Ala720=
ENST00000612452.5:c.2158_2159delinsGC	ENSP00000484033.2:p.Ala720=
ENST00000374690.7:c.2158_2159delinsGC	ENSP00000363822.3:p.Ala720=
ENST00000396043.2:c.562_563delinsGC	ENSP00000379358.2:p.Ala188=
ENST00000396044.7:c.2158_2159delinsGC	ENSP00000379359.3:p.Ala720=
ENST00000612452.4:c.1588_1589delinsGC	ENSP00000484033.1:p.Ala530=
NM_000044.3:c.2158_2159delinsGC	NP_000035.2:p.Ala720=
NM_001011645.2:c.562_563delinsGC	NP_001011645.1:p.Ala188=
NM_000044.4:c.2158_2159delinsGC	NP_000035.2:p.Ala720=
NM_001011645.3:c.562_563delinsGC	NP_001011645.1:p.Ala188=
NM_000044.6:c.2158_2159delinsGC MANE Select	NP_000035.2:p.Ala720=