Canonical Allele Identifier: CA1339183630
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240575949T= , CM000664.2:g.240575949T= GRCh38
NC_000002.11:g.241515366T= , CM000664.1:g.241515366T= GRCh37
NC_000002.10:g.241164039T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1510+339T= MANE Select ENSP00000270357.4:n.1510+339T=
ENST00000270357.8:c.817+339T= ENSP00000270357.3:n.817+339T=
ENST00000437406.1:c.109+339T= ENSP00000403319.1:n.109+339T=
ENST00000451363.5:c.151+339T= ENSP00000414661.1:n.151+339T=
ENST00000464550.5:n.346+339T=
ENST00000471657.1:n.313+339T=
ENST00000481757.5:n.1859T=
ENST00000486058.5:n.1623+339T=
ENST00000493398.5:n.656+339T=
NM_018226.4:c.1510+339T= NP_060696.4:n.1510+339T=
XM_005247036.3:c.1510+339T= XP_005247093.1:n.1510+339T=
NM_018226.5:c.1510+339T= NP_060696.4:n.1510+339T=
XM_005247036.4:c.1510+339T= XP_005247093.1:n.1510+339T=
NM_018226.6:c.1510+339T= MANE Select NP_060696.4:n.1510+339T=