Canonical Allele Identifier: CA1339183958
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576574C= , CM000664.2:g.240576574C= GRCh38
NC_000002.11:g.241515991C= , CM000664.1:g.241515991C= GRCh37
NC_000002.10:g.241164664C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1550C= MANE Select ENSP00000270357.4:p.Pro517=
ENST00000270357.8:c.857C= ENSP00000270357.3:p.Pro286=
ENST00000437406.1:c.116C= ENSP00000403319.1:p.Pro39=
ENST00000451363.5:c.191C= ENSP00000414661.1:p.Pro64=
ENST00000464550.5:n.386C=
ENST00000471657.1:n.353C=
ENST00000481757.5:n.2484C=
ENST00000486058.5:n.1663C=
ENST00000493398.5:n.696C=
NM_018226.4:c.1550C= NP_060696.4:p.Pro517=
XM_005247036.3:c.1517C= XP_005247093.1:p.Pro506=
NM_018226.5:c.1550C= NP_060696.4:p.Pro517=
XM_005247036.4:c.1517C= XP_005247093.1:p.Pro506=
NM_018226.6:c.1550C= MANE Select NP_060696.4:p.Pro517=