Canonical Allele Identifier: CA1339183722

Gene: RNPEPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576139G= , CM000664.2:g.240576139G=	GRCh38
NC_000002.11:g.241515556G= , CM000664.1:g.241515556G=	GRCh37
NC_000002.10:g.241164229G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000270357.10:c.1511-396G= MANE Select	ENSP00000270357.4:n.1511-396G=
ENST00000270357.8:c.818-396G=	ENSP00000270357.3:n.818-396G=
ENST00000437406.1:c.110-429G=	ENSP00000403319.1:n.110-429G=
ENST00000451363.5:c.152-396G=	ENSP00000414661.1:n.152-396G=
ENST00000464550.5:n.347-396G=
ENST00000471657.1:n.314-396G=
ENST00000481757.5:n.2049G=
ENST00000486058.5:n.1624-396G=
ENST00000493398.5:n.657-396G=
NM_018226.4:c.1511-396G=	NP_060696.4:n.1511-396G=
XM_005247036.3:c.1511-429G=	XP_005247093.1:n.1511-429G=
NM_018226.5:c.1511-396G=	NP_060696.4:n.1511-396G=
XM_005247036.4:c.1511-429G=	XP_005247093.1:n.1511-429G=
NM_018226.6:c.1511-396G= MANE Select	NP_060696.4:n.1511-396G=