Canonical Allele Identifier: CA2663969714
Gene: RNPEPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576620del , CM000664.2:g.240576620del GRCh38
NC_000002.11:g.241516037del , CM000664.1:g.241516037del GRCh37
NC_000002.10:g.241164710del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1596del MANE Select ENSP00000270357.4:p.Val533TrpfsTer?
ENST00000270357.8:c.903del ENSP00000270357.3:p.Val302TrpfsTer?
ENST00000437406.1:c.162del ENSP00000403319.1:p.Val55TrpfsTer?
ENST00000451363.5:c.237del ENSP00000414661.1:p.Val80TrpfsTer?
ENST00000464550.5:n.432del
ENST00000471657.1:n.399del
ENST00000481757.5:n.2530del
ENST00000486058.5:n.1709del
ENST00000493398.5:n.742del
NM_018226.4:c.1596del NP_060696.4:p.Val533TrpfsTer?
XM_005247036.3:c.1563del XP_005247093.1:p.Val522TrpfsTer?
NM_018226.5:c.1596del NP_060696.4:p.Val533TrpfsTer?
XM_005247036.4:c.1563del XP_005247093.1:p.Val522TrpfsTer?
NM_018226.6:c.1596del MANE Select NP_060696.4:p.Val533TrpfsTer?