Canonical Allele Identifier: CA1083492194
Gene: RNF145 HGNC NCBI

Linked Data

dbSNP Id: rs1784719018

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176347_159176388dup , CM000667.2:g.159176347_159176388dup GRCh38
NC_000005.9:g.158603355_158603396dup , CM000667.1:g.158603355_158603396dup GRCh37
NC_000005.8:g.158535933_158535974dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424310.7:c.621+248_621+289dup MANE Select ENSP00000409064.2:n.621+248_621+289dup
ENST00000274542.6:c.705+248_705+289dup ENSP00000274542.2:n.705+248_705+289dup
ENST00000424310.6:c.621+248_621+289dup ENSP00000409064.2:n.621+248_621+289dup
ENST00000518802.5:c.711+248_711+289dup ENSP00000430955.1:n.711+248_711+289dup
ENST00000519865.5:c.621+248_621+289dup ENSP00000430397.1:n.621+248_621+289dup
ENST00000520638.1:c.663+248_663+289dup ENSP00000429071.1:n.663+248_663+289dup
ENST00000521606.6:c.672+248_672+289dup ENSP00000430753.2:n.672+248_672+289dup
ENST00000611185.4:c.621+248_621+289dup ENSP00000482720.1:n.621+248_621+289dup
NM_001199380.1:c.711+248_711+289dup NP_001186309.1:n.711+248_711+289dup
NM_001199381.1:c.672+248_672+289dup NP_001186310.1:n.672+248_672+289dup
NM_001199382.1:c.663+248_663+289dup NP_001186311.1:n.663+248_663+289dup
NM_001199383.1:c.621+248_621+289dup NP_001186312.1:n.621+248_621+289dup
NM_144726.2:c.705+248_705+289dup NP_653327.1:n.705+248_705+289dup
XM_005265826.3:c.669+248_669+289dup XP_005265883.1:n.669+248_669+289dup
XM_017009138.2:c.621+248_621+289dup XP_016864627.1:n.621+248_621+289dup
XM_024454383.1:c.669+248_669+289dup XP_024310151.1:n.669+248_669+289dup
NM_001199381.2:c.672+248_672+289dup NP_001186310.1:n.672+248_672+289dup
NM_001199383.2:c.621+248_621+289dup MANE Select NP_001186312.1:n.621+248_621+289dup
NM_001199380.2:c.711+248_711+289dup NP_001186309.1:n.711+248_711+289dup
NM_001199382.2:c.663+248_663+289dup NP_001186311.1:n.663+248_663+289dup
NM_144726.3:c.705+248_705+289dup NP_653327.1:n.705+248_705+289dup