Canonical Allele Identifier: CA1339183912

Gene: RNPEPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576464T= , CM000664.2:g.240576464T=	GRCh38
NC_000002.11:g.241515881T= , CM000664.1:g.241515881T=	GRCh37
NC_000002.10:g.241164554T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1511-71T= MANE Select	ENSP00000270357.4:n.1511-71T=
ENST00000270357.8:c.818-71T=	ENSP00000270357.3:n.818-71T=
ENST00000437406.1:c.110-104T=	ENSP00000403319.1:n.110-104T=
ENST00000451363.5:c.152-71T=	ENSP00000414661.1:n.152-71T=
ENST00000464550.5:n.347-71T=
ENST00000471657.1:n.314-71T=
ENST00000481757.5:n.2374T=
ENST00000486058.5:n.1624-71T=
ENST00000493398.5:n.657-71T=
NM_018226.4:c.1511-71T=	NP_060696.4:n.1511-71T=
XM_005247036.3:c.1511-104T=	XP_005247093.1:n.1511-104T=
NM_018226.5:c.1511-71T=	NP_060696.4:n.1511-71T=
XM_005247036.4:c.1511-104T=	XP_005247093.1:n.1511-104T=
NM_018226.6:c.1511-71T= MANE Select	NP_060696.4:n.1511-71T=