Canonical Allele Identifier: CA1594977516
Gene: RNF145 HGNC NCBI

Linked Data

dbSNP Id: rs1784720601

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159176375_159176376dup , CM000667.2:g.159176375_159176376dup GRCh38
NC_000005.9:g.158603383_158603384dup , CM000667.1:g.158603383_158603384dup GRCh37
NC_000005.8:g.158535961_158535962dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000424310.7:c.621+259_621+260dup MANE Select ENSP00000409064.2:n.621+259_621+260dup
ENST00000274542.6:c.705+259_705+260dup ENSP00000274542.2:n.705+259_705+260dup
ENST00000424310.6:c.621+259_621+260dup ENSP00000409064.2:n.621+259_621+260dup
ENST00000518802.5:c.711+259_711+260dup ENSP00000430955.1:n.711+259_711+260dup
ENST00000519865.5:c.621+259_621+260dup ENSP00000430397.1:n.621+259_621+260dup
ENST00000520638.1:c.663+259_663+260dup ENSP00000429071.1:n.663+259_663+260dup
ENST00000521606.6:c.672+259_672+260dup ENSP00000430753.2:n.672+259_672+260dup
ENST00000611185.4:c.621+259_621+260dup ENSP00000482720.1:n.621+259_621+260dup
NM_001199380.1:c.711+259_711+260dup NP_001186309.1:n.711+259_711+260dup
NM_001199381.1:c.672+259_672+260dup NP_001186310.1:n.672+259_672+260dup
NM_001199382.1:c.663+259_663+260dup NP_001186311.1:n.663+259_663+260dup
NM_001199383.1:c.621+259_621+260dup NP_001186312.1:n.621+259_621+260dup
NM_144726.2:c.705+259_705+260dup NP_653327.1:n.705+259_705+260dup
XM_005265826.3:c.669+259_669+260dup XP_005265883.1:n.669+259_669+260dup
XM_017009138.2:c.621+259_621+260dup XP_016864627.1:n.621+259_621+260dup
XM_024454383.1:c.669+259_669+260dup XP_024310151.1:n.669+259_669+260dup
NM_001199381.2:c.672+259_672+260dup NP_001186310.1:n.672+259_672+260dup
NM_001199383.2:c.621+259_621+260dup MANE Select NP_001186312.1:n.621+259_621+260dup
NM_001199380.2:c.711+259_711+260dup NP_001186309.1:n.711+259_711+260dup
NM_001199382.2:c.663+259_663+260dup NP_001186311.1:n.663+259_663+260dup
NM_144726.3:c.705+259_705+260dup NP_653327.1:n.705+259_705+260dup