Canonical Allele Identifier: CA1339183682
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576039A= , CM000664.2:g.240576039A= GRCh38
NC_000002.11:g.241515456A= , CM000664.1:g.241515456A= GRCh37
NC_000002.10:g.241164129A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270357.10:c.1510+429A= MANE Select ENSP00000270357.4:n.1510+429A=
ENST00000270357.8:c.817+429A= ENSP00000270357.3:n.817+429A=
ENST00000437406.1:c.109+429A= ENSP00000403319.1:n.109+429A=
ENST00000451363.5:c.151+429A= ENSP00000414661.1:n.151+429A=
ENST00000464550.5:n.346+429A=
ENST00000471657.1:n.313+429A=
ENST00000481757.5:n.1949A=
ENST00000486058.5:n.1623+429A=
ENST00000493398.5:n.656+429A=
NM_018226.4:c.1510+429A= NP_060696.4:n.1510+429A=
XM_005247036.3:c.1510+429A= XP_005247093.1:n.1510+429A=
NM_018226.5:c.1510+429A= NP_060696.4:n.1510+429A=
XM_005247036.4:c.1510+429A= XP_005247093.1:n.1510+429A=
NM_018226.6:c.1510+429A= MANE Select NP_060696.4:n.1510+429A=