Canonical Allele Identifier: CA432232452

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516032C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576615C>A , CM000664.2:g.240576615C>A	GRCh38
NC_000002.11:g.241516032C>A , CM000664.1:g.241516032C>A	GRCh37
NC_000002.10:g.241164705C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1591C>A MANE Select	ENSP00000270357.4:p.Arg531=
ENST00000270357.8:c.898C>A	ENSP00000270357.3:p.Arg300=
ENST00000437406.1:c.157C>A	ENSP00000403319.1:p.Arg53=
ENST00000451363.5:c.232C>A	ENSP00000414661.1:p.Arg78=
ENST00000464550.5:n.427C>A
ENST00000471657.1:n.394C>A
ENST00000481757.5:n.2525C>A
ENST00000486058.5:n.1704C>A
ENST00000493398.5:n.737C>A
NM_018226.4:c.1591C>A	NP_060696.4:p.Arg531=
XM_005247036.3:c.1558C>A	XP_005247093.1:p.Arg520=
NM_018226.5:c.1591C>A	NP_060696.4:p.Arg531=
XM_005247036.4:c.1558C>A	XP_005247093.1:p.Arg520=
NM_018226.6:c.1591C>A MANE Select	NP_060696.4:p.Arg531=