Canonical Allele Identifier: CA1339183697
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576077T= , CM000664.2:g.240576077T= GRCh38
NC_000002.11:g.241515494T= , CM000664.1:g.241515494T= GRCh37
NC_000002.10:g.241164167T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-458T= MANE Select ENSP00000270357.4:n.1511-458T=
ENST00000270357.8:c.818-458T= ENSP00000270357.3:n.818-458T=
ENST00000437406.1:c.109+467T= ENSP00000403319.1:n.109+467T=
ENST00000451363.5:c.152-458T= ENSP00000414661.1:n.152-458T=
ENST00000464550.5:n.347-458T=
ENST00000471657.1:n.314-458T=
ENST00000481757.5:n.1987T=
ENST00000486058.5:n.1624-458T=
ENST00000493398.5:n.657-458T=
NM_018226.4:c.1511-458T= NP_060696.4:n.1511-458T=
XM_005247036.3:c.1510+467T= XP_005247093.1:n.1510+467T=
NM_018226.5:c.1511-458T= NP_060696.4:n.1511-458T=
XM_005247036.4:c.1510+467T= XP_005247093.1:n.1510+467T=
NM_018226.6:c.1511-458T= MANE Select NP_060696.4:n.1511-458T=