Canonical Allele Identifier: CA1339183931

Gene: RNPEPL1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576522T= , CM000664.2:g.240576522T=	GRCh38
NC_000002.11:g.241515939T= , CM000664.1:g.241515939T=	GRCh37
NC_000002.10:g.241164612T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1511-13T= MANE Select	ENSP00000270357.4:n.1511-13T=
ENST00000270357.8:c.818-13T=	ENSP00000270357.3:n.818-13T=
ENST00000437406.1:c.110-46T=	ENSP00000403319.1:n.110-46T=
ENST00000451363.5:c.152-13T=	ENSP00000414661.1:n.152-13T=
ENST00000464550.5:n.347-13T=
ENST00000471657.1:n.314-13T=
ENST00000481757.5:n.2432T=
ENST00000486058.5:n.1624-13T=
ENST00000493398.5:n.657-13T=
NM_018226.4:c.1511-13T=	NP_060696.4:n.1511-13T=
XM_005247036.3:c.1511-46T=	XP_005247093.1:n.1511-46T=
NM_018226.5:c.1511-13T=	NP_060696.4:n.1511-13T=
XM_005247036.4:c.1511-46T=	XP_005247093.1:n.1511-46T=
NM_018226.6:c.1511-13T= MANE Select	NP_060696.4:n.1511-13T=