Canonical Allele Identifier: CA1339183793
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576241A= , CM000664.2:g.240576241A= GRCh38
NC_000002.11:g.241515658A= , CM000664.1:g.241515658A= GRCh37
NC_000002.10:g.241164331A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270357.10:c.1511-294A= MANE Select ENSP00000270357.4:n.1511-294A=
ENST00000270357.8:c.818-294A= ENSP00000270357.3:n.818-294A=
ENST00000437406.1:c.110-327A= ENSP00000403319.1:n.110-327A=
ENST00000451363.5:c.152-294A= ENSP00000414661.1:n.152-294A=
ENST00000464550.5:n.347-294A=
ENST00000471657.1:n.314-294A=
ENST00000481757.5:n.2151A=
ENST00000486058.5:n.1624-294A=
ENST00000493398.5:n.657-294A=
NM_018226.4:c.1511-294A= NP_060696.4:n.1511-294A=
XM_005247036.3:c.1511-327A= XP_005247093.1:n.1511-327A=
NM_018226.5:c.1511-294A= NP_060696.4:n.1511-294A=
XM_005247036.4:c.1511-327A= XP_005247093.1:n.1511-327A=
NM_018226.6:c.1511-294A= MANE Select NP_060696.4:n.1511-294A=