Canonical Allele Identifier: CA1339183791
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576240G= , CM000664.2:g.240576240G= GRCh38
NC_000002.11:g.241515657G= , CM000664.1:g.241515657G= GRCh37
NC_000002.10:g.241164330G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270357.10:c.1511-295G= MANE Select ENSP00000270357.4:n.1511-295G=
ENST00000270357.8:c.818-295G= ENSP00000270357.3:n.818-295G=
ENST00000437406.1:c.110-328G= ENSP00000403319.1:n.110-328G=
ENST00000451363.5:c.152-295G= ENSP00000414661.1:n.152-295G=
ENST00000464550.5:n.347-295G=
ENST00000471657.1:n.314-295G=
ENST00000481757.5:n.2150G=
ENST00000486058.5:n.1624-295G=
ENST00000493398.5:n.657-295G=
NM_018226.4:c.1511-295G= NP_060696.4:n.1511-295G=
XM_005247036.3:c.1511-328G= XP_005247093.1:n.1511-328G=
NM_018226.5:c.1511-295G= NP_060696.4:n.1511-295G=
XM_005247036.4:c.1511-328G= XP_005247093.1:n.1511-328G=
NM_018226.6:c.1511-295G= MANE Select NP_060696.4:n.1511-295G=