Canonical Allele Identifier: CA1339183908
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576450C= , CM000664.2:g.240576450C= GRCh38
NC_000002.11:g.241515867C= , CM000664.1:g.241515867C= GRCh37
NC_000002.10:g.241164540C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-85C= MANE Select ENSP00000270357.4:n.1511-85C=
ENST00000270357.8:c.818-85C= ENSP00000270357.3:n.818-85C=
ENST00000437406.1:c.110-118C= ENSP00000403319.1:n.110-118C=
ENST00000451363.5:c.152-85C= ENSP00000414661.1:n.152-85C=
ENST00000464550.5:n.347-85C=
ENST00000471657.1:n.314-85C=
ENST00000481757.5:n.2360C=
ENST00000486058.5:n.1624-85C=
ENST00000493398.5:n.657-85C=
NM_018226.4:c.1511-85C= NP_060696.4:n.1511-85C=
XM_005247036.3:c.1511-118C= XP_005247093.1:n.1511-118C=
NM_018226.5:c.1511-85C= NP_060696.4:n.1511-85C=
XM_005247036.4:c.1511-118C= XP_005247093.1:n.1511-118C=
NM_018226.6:c.1511-85C= MANE Select NP_060696.4:n.1511-85C=