Canonical Allele Identifier: CA2435134237
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67721649A= , CM000685.2:g.67721649A= GRCh38
NC_000023.10:g.66941491A= , CM000685.1:g.66941491A= GRCh37
NC_000023.9:g.66858216A= NCBI36
NG_009014.2:g.182618A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396043.4:c.*667-184A= ENSP00000379358.4:n.*667-184A=
ENST00000374690.9:c.2319-184A= MANE Select ENSP00000363822.3:n.2319-184A=
ENST00000396043.3:c.946-184A= ENSP00000379358.3:n.946-184A=
ENST00000396044.8:c.2174-2037A= ENSP00000379359.3:n.2174-2037A=
ENST00000612452.5:c.2319-184A= ENSP00000484033.2:n.2319-184A=
ENST00000374690.7:c.2319-184A= ENSP00000363822.3:n.2319-184A=
ENST00000396043.2:c.723-184A= ENSP00000379358.2:n.723-184A=
ENST00000396044.7:c.2174-2037A= ENSP00000379359.3:n.2174-2037A=
ENST00000612452.4:c.1749-184A= ENSP00000484033.1:n.1749-184A=
NM_000044.3:c.2319-184A= NP_000035.2:n.2319-184A=
NM_001011645.2:c.723-184A= NP_001011645.1:n.723-184A=
NM_000044.4:c.2319-184A= NP_000035.2:n.2319-184A=
NM_001011645.3:c.723-184A= NP_001011645.1:n.723-184A=
NM_000044.6:c.2319-184A= MANE Select NP_000035.2:n.2319-184A=