Canonical Allele Identifier: CA2435066386
Gene: AR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.67545813G= , CM000685.2:g.67545813G= GRCh38
NC_000023.10:g.66765655G= , CM000685.1:g.66765655G= GRCh37
NC_000023.9:g.66682380G= NCBI36
NG_009014.2:g.6782G=

Transcript Alleles

HGVS Amino-acid change
ENST00000396043.4:c.667G= ENSP00000379358.4:p.Asp223=
ENST00000374690.9:c.667G= MANE Select ENSP00000363822.3:p.Asp223=
ENST00000396044.8:c.667G= ENSP00000379359.3:p.Asp223=
ENST00000612452.5:c.667G= ENSP00000484033.2:p.Asp223=
ENST00000374690.7:c.667G= ENSP00000363822.3:p.Asp223=
ENST00000396044.7:c.667G= ENSP00000379359.3:p.Asp223=
ENST00000504326.5:c.667G= ENSP00000421155.1:p.Asp223=
ENST00000513847.5:n.994G=
ENST00000514029.5:c.667G= ENSP00000425199.1:p.Asp223=
ENST00000612010.4:c.667G= ENSP00000482407.1:p.Asp223=
ENST00000612452.4:c.97G= ENSP00000484033.1:p.Asp33=
ENST00000613054.2:c.667G= ENSP00000479013.1:p.Asp223=
NM_000044.3:c.667G= NP_000035.2:p.Asp223=
NM_000044.4:c.667G= NP_000035.2:p.Asp223=
NM_001011645.3:c.-1117G= NP_001011645.1:n.-1117G=
NM_001348061.1:c.667G= NP_001334990.1:p.Asp223=
NM_001348063.1:c.667G= NP_001334992.1:p.Asp223=
NM_001348064.1:c.667G= NP_001334993.1:p.Asp223=
NM_000044.6:c.667G= MANE Select NP_000035.2:p.Asp223=