Canonical Allele Identifier: CA1339183910
Gene: RNPEPL1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576457T= , CM000664.2:g.240576457T= GRCh38
NC_000002.11:g.241515874T= , CM000664.1:g.241515874T= GRCh37
NC_000002.10:g.241164547T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-78T= MANE Select ENSP00000270357.4:n.1511-78T=
ENST00000270357.8:c.818-78T= ENSP00000270357.3:n.818-78T=
ENST00000437406.1:c.110-111T= ENSP00000403319.1:n.110-111T=
ENST00000451363.5:c.152-78T= ENSP00000414661.1:n.152-78T=
ENST00000464550.5:n.347-78T=
ENST00000471657.1:n.314-78T=
ENST00000481757.5:n.2367T=
ENST00000486058.5:n.1624-78T=
ENST00000493398.5:n.657-78T=
NM_018226.4:c.1511-78T= NP_060696.4:n.1511-78T=
XM_005247036.3:c.1511-111T= XP_005247093.1:n.1511-111T=
NM_018226.5:c.1511-78T= NP_060696.4:n.1511-78T=
XM_005247036.4:c.1511-111T= XP_005247093.1:n.1511-111T=
NM_018226.6:c.1511-78T= MANE Select NP_060696.4:n.1511-78T=
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