Canonical Allele Identifier: CA1339183724
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576141A= , CM000664.2:g.240576141A= GRCh38
NC_000002.11:g.241515558A= , CM000664.1:g.241515558A= GRCh37
NC_000002.10:g.241164231A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270357.10:c.1511-394A= MANE Select ENSP00000270357.4:n.1511-394A=
ENST00000270357.8:c.818-394A= ENSP00000270357.3:n.818-394A=
ENST00000437406.1:c.110-427A= ENSP00000403319.1:n.110-427A=
ENST00000451363.5:c.152-394A= ENSP00000414661.1:n.152-394A=
ENST00000464550.5:n.347-394A=
ENST00000471657.1:n.314-394A=
ENST00000481757.5:n.2051A=
ENST00000486058.5:n.1624-394A=
ENST00000493398.5:n.657-394A=
NM_018226.4:c.1511-394A= NP_060696.4:n.1511-394A=
XM_005247036.3:c.1511-427A= XP_005247093.1:n.1511-427A=
NM_018226.5:c.1511-394A= NP_060696.4:n.1511-394A=
XM_005247036.4:c.1511-427A= XP_005247093.1:n.1511-427A=
NM_018226.6:c.1511-394A= MANE Select NP_060696.4:n.1511-394A=