Canonical Allele Identifier: CA1339183916

Gene: RNPEPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576469G= , CM000664.2:g.240576469G=	GRCh38
NC_000002.11:g.241515886G= , CM000664.1:g.241515886G=	GRCh37
NC_000002.10:g.241164559G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1511-66G= MANE Select	ENSP00000270357.4:n.1511-66G=
ENST00000270357.8:c.818-66G=	ENSP00000270357.3:n.818-66G=
ENST00000437406.1:c.110-99G=	ENSP00000403319.1:n.110-99G=
ENST00000451363.5:c.152-66G=	ENSP00000414661.1:n.152-66G=
ENST00000464550.5:n.347-66G=
ENST00000471657.1:n.314-66G=
ENST00000481757.5:n.2379G=
ENST00000486058.5:n.1624-66G=
ENST00000493398.5:n.657-66G=
NM_018226.4:c.1511-66G=	NP_060696.4:n.1511-66G=
XM_005247036.3:c.1511-99G=	XP_005247093.1:n.1511-99G=
NM_018226.5:c.1511-66G=	NP_060696.4:n.1511-66G=
XM_005247036.4:c.1511-99G=	XP_005247093.1:n.1511-99G=
NM_018226.6:c.1511-66G= MANE Select	NP_060696.4:n.1511-66G=