Canonical Allele Identifier: CA2435134319
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721823T= , CM000685.2:g.67721823T= GRCh38
NC_000023.10:g.66941665T= , CM000685.1:g.66941665T= GRCh37
NC_000023.9:g.66858390T= NCBI36
NG_009014.2:g.182792T=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.*667-10T= ENSP00000379358.4:n.*667-10T=
ENST00000374690.9:c.2319-10T= MANE Select ENSP00000363822.3:n.2319-10T=
ENST00000396043.3:c.946-10T= ENSP00000379358.3:n.946-10T=
ENST00000396044.8:c.2174-1863T= ENSP00000379359.3:n.2174-1863T=
ENST00000612452.5:c.2319-10T= ENSP00000484033.2:n.2319-10T=
ENST00000374690.7:c.2319-10T= ENSP00000363822.3:n.2319-10T=
ENST00000396043.2:c.723-10T= ENSP00000379358.2:n.723-10T=
ENST00000396044.7:c.2174-1863T= ENSP00000379359.3:n.2174-1863T=
ENST00000612452.4:c.1749-10T= ENSP00000484033.1:n.1749-10T=
NM_000044.3:c.2319-10T= NP_000035.2:n.2319-10T=
NM_001011645.2:c.723-10T= NP_001011645.1:n.723-10T=
NM_000044.4:c.2319-10T= NP_000035.2:n.2319-10T=
NM_001011645.3:c.723-10T= NP_001011645.1:n.723-10T=
NM_000044.6:c.2319-10T= MANE Select NP_000035.2:n.2319-10T=