Canonical Allele Identifier: CA399203112
Gene: RNF135 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30998764G>T , CM000679.2:g.30998764G>T GRCh38
NC_000017.10:g.29325782G>T , CM000679.1:g.29325782G>T GRCh37
NC_000017.9:g.26349908G>T NCBI36
NG_011701.1:g.32827G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328381.10:c.872G>T MANE Select ENSP00000328340.5:p.Arg291Leu
ENST00000324689.8:c.*76G>T ENSP00000323693.4:n.*76G>T
ENST00000328381.9:c.872G>T ENSP00000328340.5:p.Arg291Leu
ENST00000443677.6:c.*76G>T ENSP00000411965.2:n.*76G>T
ENST00000535306.6:c.*76G>T ENSP00000440470.2:n.*76G>T
NM_001184992.1:c.*76G>T NP_001171921.1:n.*76G>T
NM_032322.3:c.872G>T NP_115698.3:p.Arg291Leu
NM_197939.1:c.*76G>T NP_922921.1:n.*76G>T
XM_005258043.3:c.329G>T XP_005258100.1:p.Arg110Leu
XM_006722138.2:c.551G>T XP_006722201.1:p.Arg184Leu
XM_017025223.1:c.329G>T XP_016880712.1:p.Arg110Leu
XM_024451000.1:c.329G>T XP_024306768.1:p.Arg110Leu
XM_024451001.1:c.329G>T XP_024306769.1:p.Arg110Leu
XR_002958077.1:n.1140G>T
NM_032322.4:c.872G>T MANE Select NP_115698.3:p.Arg291Leu
NM_001184992.2:c.*76G>T NP_001171921.1:n.*76G>T
NM_197939.2:c.*76G>T NP_922921.1:n.*76G>T