Canonical Allele Identifier: CA432232395

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516007C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576590C>T , CM000664.2:g.240576590C>T	GRCh38
NC_000002.11:g.241516007C>T , CM000664.1:g.241516007C>T	GRCh37
NC_000002.10:g.241164680C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1566C>T MANE Select	ENSP00000270357.4:p.Asp522=
ENST00000270357.8:c.873C>T	ENSP00000270357.3:p.Asp291=
ENST00000437406.1:c.132C>T	ENSP00000403319.1:p.Asp44=
ENST00000451363.5:c.207C>T	ENSP00000414661.1:p.Asp69=
ENST00000464550.5:n.402C>T
ENST00000471657.1:n.369C>T
ENST00000481757.5:n.2500C>T
ENST00000486058.5:n.1679C>T
ENST00000493398.5:n.712C>T
NM_018226.4:c.1566C>T	NP_060696.4:p.Asp522=
XM_005247036.3:c.1533C>T	XP_005247093.1:p.Asp511=
NM_018226.5:c.1566C>T	NP_060696.4:p.Asp522=
XM_005247036.4:c.1533C>T	XP_005247093.1:p.Asp511=
NM_018226.6:c.1566C>T MANE Select	NP_060696.4:p.Asp522=