Canonical Allele Identifier: CA1339183764
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576197C= , CM000664.2:g.240576197C= GRCh38
NC_000002.11:g.241515614C= , CM000664.1:g.241515614C= GRCh37
NC_000002.10:g.241164287C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270357.10:c.1511-338C= MANE Select ENSP00000270357.4:n.1511-338C=
ENST00000270357.8:c.818-338C= ENSP00000270357.3:n.818-338C=
ENST00000437406.1:c.110-371C= ENSP00000403319.1:n.110-371C=
ENST00000451363.5:c.152-338C= ENSP00000414661.1:n.152-338C=
ENST00000464550.5:n.347-338C=
ENST00000471657.1:n.314-338C=
ENST00000481757.5:n.2107C=
ENST00000486058.5:n.1624-338C=
ENST00000493398.5:n.657-338C=
NM_018226.4:c.1511-338C= NP_060696.4:n.1511-338C=
XM_005247036.3:c.1511-371C= XP_005247093.1:n.1511-371C=
NM_018226.5:c.1511-338C= NP_060696.4:n.1511-338C=
XM_005247036.4:c.1511-371C= XP_005247093.1:n.1511-371C=
NM_018226.6:c.1511-338C= MANE Select NP_060696.4:n.1511-338C=