Canonical Allele Identifier: CA2255462498
Gene: RNF135 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30998756A= , CM000679.2:g.30998756A= GRCh38
NC_000017.10:g.29325774A= , CM000679.1:g.29325774A= GRCh37
NC_000017.9:g.26349900A= NCBI36
NG_011701.1:g.32819A=

Transcript Alleles

HGVS Amino-acid change
ENST00000328381.10:c.864A= MANE Select ENSP00000328340.5:p.Gln288=
ENST00000324689.8:c.*68A= ENSP00000323693.4:n.*68A=
ENST00000328381.9:c.864A= ENSP00000328340.5:p.Gln288=
ENST00000443677.6:c.*68A= ENSP00000411965.2:n.*68A=
ENST00000535306.6:c.*68A= ENSP00000440470.2:n.*68A=
NM_001184992.1:c.*68A= NP_001171921.1:n.*68A=
NM_032322.3:c.864A= NP_115698.3:p.Gln288=
NM_197939.1:c.*68A= NP_922921.1:n.*68A=
XM_005258043.3:c.321A= XP_005258100.1:p.Gln107=
XM_006722138.2:c.543A= XP_006722201.1:p.Gln181=
XM_017025223.1:c.321A= XP_016880712.1:p.Gln107=
XM_024451000.1:c.321A= XP_024306768.1:p.Gln107=
XM_024451001.1:c.321A= XP_024306769.1:p.Gln107=
XR_002958077.1:n.1132A=
NM_032322.4:c.864A= MANE Select NP_115698.3:p.Gln288=
NM_001184992.2:c.*68A= NP_001171921.1:n.*68A=
NM_197939.2:c.*68A= NP_922921.1:n.*68A=