Canonical Allele Identifier: CA2435134709
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67722721C= , CM000685.2:g.67722721C= GRCh38
NC_000023.10:g.66942563C= , CM000685.1:g.66942563C= GRCh37
NC_000023.9:g.66859288C= NCBI36
NG_009014.2:g.183690C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*798-106C= ENSP00000379358.4:n.*798-106C=
ENST00000374690.9:c.2450-106C= MANE Select ENSP00000363822.3:n.2450-106C=
ENST00000396043.3:c.1077-106C= ENSP00000379358.3:n.1077-106C=
ENST00000396044.8:c.2174-965C= ENSP00000379359.3:n.2174-965C=
ENST00000612452.5:c.2450-106C= ENSP00000484033.2:n.2450-106C=
ENST00000374690.7:c.2450-106C= ENSP00000363822.3:n.2450-106C=
ENST00000396043.2:c.854-106C= ENSP00000379358.2:n.854-106C=
ENST00000396044.7:c.2174-965C= ENSP00000379359.3:n.2174-965C=
ENST00000612452.4:c.1901-106C= ENSP00000484033.1:n.1901-106C=
NM_000044.3:c.2450-106C= NP_000035.2:n.2450-106C=
NM_001011645.2:c.854-106C= NP_001011645.1:n.854-106C=
NM_000044.4:c.2450-106C= NP_000035.2:n.2450-106C=
NM_001011645.3:c.854-106C= NP_001011645.1:n.854-106C=
NM_000044.6:c.2450-106C= MANE Select NP_000035.2:n.2450-106C=