Canonical Allele Identifier: CA2663966507
Gene: RNPEPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240575913del , CM000664.2:g.240575913del GRCh38
NC_000002.11:g.241515330del , CM000664.1:g.241515330del GRCh37
NC_000002.10:g.241164003del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1510+303del MANE Select ENSP00000270357.4:n.1510+303del
ENST00000270357.8:c.817+303del ENSP00000270357.3:n.817+303del
ENST00000437406.1:c.109+303del ENSP00000403319.1:n.109+303del
ENST00000451363.5:c.151+303del ENSP00000414661.1:n.151+303del
ENST00000464550.5:n.346+303del
ENST00000471657.1:n.313+303del
ENST00000481757.5:n.1823del
ENST00000486058.5:n.1623+303del
ENST00000493398.5:n.656+303del
NM_018226.4:c.1510+303del NP_060696.4:n.1510+303del
XM_005247036.3:c.1510+303del XP_005247093.1:n.1510+303del
NM_018226.5:c.1510+303del NP_060696.4:n.1510+303del
XM_005247036.4:c.1510+303del XP_005247093.1:n.1510+303del
NM_018226.6:c.1510+303del MANE Select NP_060696.4:n.1510+303del