Canonical Allele Identifier: CA351286335

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516069A>T (hg19) ; chr2:g.240576652A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576652A>T , CM000664.2:g.240576652A>T	GRCh38
NC_000002.11:g.241516069A>T , CM000664.1:g.241516069A>T	GRCh37
NC_000002.10:g.241164742A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1628A>T MANE Select	ENSP00000270357.4:p.Glu543Val
ENST00000270357.8:c.935A>T	ENSP00000270357.3:p.Glu312Val
ENST00000437406.1:c.194A>T	ENSP00000403319.1:p.Glu65Val
ENST00000451363.5:c.269A>T	ENSP00000414661.1:p.Glu90Val
ENST00000464550.5:n.464A>T
ENST00000471657.1:n.431A>T
ENST00000481757.5:n.2562A>T
ENST00000486058.5:n.1741A>T
ENST00000493398.5:n.774A>T
NM_018226.4:c.1628A>T	NP_060696.4:p.Glu543Val
XM_005247036.3:c.1595A>T	XP_005247093.1:p.Glu532Val
NM_018226.5:c.1628A>T	NP_060696.4:p.Glu543Val
XM_005247036.4:c.1595A>T	XP_005247093.1:p.Glu532Val
NM_018226.6:c.1628A>T MANE Select	NP_060696.4:p.Glu543Val