Canonical Allele Identifier: CA351285867

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241515965G>T (hg19) ; chr2:g.240576548G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576548G>T , CM000664.2:g.240576548G>T	GRCh38
NC_000002.11:g.241515965G>T , CM000664.1:g.241515965G>T	GRCh37
NC_000002.10:g.241164638G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1524G>T MANE Select	ENSP00000270357.4:p.Glu508Asp
ENST00000270357.8:c.831G>T	ENSP00000270357.3:p.Glu277Asp
ENST00000437406.1:c.110-20G>T	ENSP00000403319.1:n.110-20G>T
ENST00000451363.5:c.165G>T	ENSP00000414661.1:p.Glu55Asp
ENST00000464550.5:n.360G>T
ENST00000471657.1:n.327G>T
ENST00000481757.5:n.2458G>T
ENST00000486058.5:n.1637G>T
ENST00000493398.5:n.670G>T
NM_018226.4:c.1524G>T	NP_060696.4:p.Glu508Asp
XM_005247036.3:c.1511-20G>T	XP_005247093.1:n.1511-20G>T
NM_018226.5:c.1524G>T	NP_060696.4:p.Glu508Asp
XM_005247036.4:c.1511-20G>T	XP_005247093.1:n.1511-20G>T
NM_018226.6:c.1524G>T MANE Select	NP_060696.4:p.Glu508Asp