Canonical Allele Identifier: CA1339183817
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576280G= , CM000664.2:g.240576280G= GRCh38
NC_000002.11:g.241515697G= , CM000664.1:g.241515697G= GRCh37
NC_000002.10:g.241164370G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-255G= MANE Select ENSP00000270357.4:n.1511-255G=
ENST00000270357.8:c.818-255G= ENSP00000270357.3:n.818-255G=
ENST00000437406.1:c.110-288G= ENSP00000403319.1:n.110-288G=
ENST00000451363.5:c.152-255G= ENSP00000414661.1:n.152-255G=
ENST00000464550.5:n.347-255G=
ENST00000471657.1:n.314-255G=
ENST00000481757.5:n.2190G=
ENST00000486058.5:n.1624-255G=
ENST00000493398.5:n.657-255G=
NM_018226.4:c.1511-255G= NP_060696.4:n.1511-255G=
XM_005247036.3:c.1511-288G= XP_005247093.1:n.1511-288G=
NM_018226.5:c.1511-255G= NP_060696.4:n.1511-255G=
XM_005247036.4:c.1511-288G= XP_005247093.1:n.1511-288G=
NM_018226.6:c.1511-255G= MANE Select NP_060696.4:n.1511-255G=