Canonical Allele Identifier: CA1594977617
Gene: RNF145 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176593G= , CM000667.2:g.159176593G= GRCh38
NC_000005.9:g.158603601G= , CM000667.1:g.158603601G= GRCh37
NC_000005.8:g.158536179G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000424310.7:c.621+39C= MANE Select ENSP00000409064.2:n.621+39C=
ENST00000274542.6:c.705+39C= ENSP00000274542.2:n.705+39C=
ENST00000424310.6:c.621+39C= ENSP00000409064.2:n.621+39C=
ENST00000518802.5:c.711+39C= ENSP00000430955.1:n.711+39C=
ENST00000519865.5:c.621+39C= ENSP00000430397.1:n.621+39C=
ENST00000520638.1:c.663+39C= ENSP00000429071.1:n.663+39C=
ENST00000521606.6:c.672+39C= ENSP00000430753.2:n.672+39C=
ENST00000611185.4:c.621+39C= ENSP00000482720.1:n.621+39C=
NM_001199380.1:c.711+39C= NP_001186309.1:n.711+39C=
NM_001199381.1:c.672+39C= NP_001186310.1:n.672+39C=
NM_001199382.1:c.663+39C= NP_001186311.1:n.663+39C=
NM_001199383.1:c.621+39C= NP_001186312.1:n.621+39C=
NM_144726.2:c.705+39C= NP_653327.1:n.705+39C=
XM_005265826.3:c.669+39C= XP_005265883.1:n.669+39C=
XM_017009138.2:c.621+39C= XP_016864627.1:n.621+39C=
XM_024454383.1:c.669+39C= XP_024310151.1:n.669+39C=
NM_001199381.2:c.672+39C= NP_001186310.1:n.672+39C=
NM_001199383.2:c.621+39C= MANE Select NP_001186312.1:n.621+39C=
NM_001199380.2:c.711+39C= NP_001186309.1:n.711+39C=
NM_001199382.2:c.663+39C= NP_001186311.1:n.663+39C=
NM_144726.3:c.705+39C= NP_653327.1:n.705+39C=