Canonical Allele Identifier: CA1339183960
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576576C= , CM000664.2:g.240576576C= GRCh38
NC_000002.11:g.241515993C= , CM000664.1:g.241515993C= GRCh37
NC_000002.10:g.241164666C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1552C= MANE Select ENSP00000270357.4:p.Leu518=
ENST00000270357.8:c.859C= ENSP00000270357.3:p.Leu287=
ENST00000437406.1:c.118C= ENSP00000403319.1:p.Leu40=
ENST00000451363.5:c.193C= ENSP00000414661.1:p.Leu65=
ENST00000464550.5:n.388C=
ENST00000471657.1:n.355C=
ENST00000481757.5:n.2486C=
ENST00000486058.5:n.1665C=
ENST00000493398.5:n.698C=
NM_018226.4:c.1552C= NP_060696.4:p.Leu518=
XM_005247036.3:c.1519C= XP_005247093.1:p.Leu507=
NM_018226.5:c.1552C= NP_060696.4:p.Leu518=
XM_005247036.4:c.1519C= XP_005247093.1:p.Leu507=
NM_018226.6:c.1552C= MANE Select NP_060696.4:p.Leu518=