Canonical Allele Identifier: CA3012298955

Gene: RNPEPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576192_240576193del , CM000664.2:g.240576192_240576193del	GRCh38
NC_000002.11:g.241515609_241515610del , CM000664.1:g.241515609_241515610del	GRCh37
NC_000002.10:g.241164282_241164283del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1511-343_1511-342del MANE Select	ENSP00000270357.4:n.1511-343_1511-342del
ENST00000270357.8:c.818-343_818-342del	ENSP00000270357.3:n.818-343_818-342del
ENST00000437406.1:c.110-376_110-375del	ENSP00000403319.1:n.110-376_110-375del
ENST00000451363.5:c.152-343_152-342del	ENSP00000414661.1:n.152-343_152-342del
ENST00000464550.5:n.347-343_347-342del
ENST00000471657.1:n.314-343_314-342del
ENST00000481757.5:n.2102_2103del
ENST00000486058.5:n.1624-343_1624-342del
ENST00000493398.5:n.657-343_657-342del
NM_018226.4:c.1511-343_1511-342del	NP_060696.4:n.1511-343_1511-342del
XM_005247036.3:c.1511-376_1511-375del	XP_005247093.1:n.1511-376_1511-375del
NM_018226.5:c.1511-343_1511-342del	NP_060696.4:n.1511-343_1511-342del
XM_005247036.4:c.1511-376_1511-375del	XP_005247093.1:n.1511-376_1511-375del
NM_018226.6:c.1511-343_1511-342del MANE Select	NP_060696.4:n.1511-343_1511-342del