Canonical Allele Identifier: CA351286202

Gene: RNPEPL1

Linked Data

• dbSNP Id: rs2093038393
• MyVariant Identifiers: chr2:g.241516044G>A (hg19) ; chr2:g.240576627G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576627G>A , CM000664.2:g.240576627G>A	GRCh38
NC_000002.11:g.241516044G>A , CM000664.1:g.241516044G>A	GRCh37
NC_000002.10:g.241164717G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1603G>A MANE Select	ENSP00000270357.4:p.Ala535Thr
ENST00000270357.8:c.910G>A	ENSP00000270357.3:p.Ala304Thr
ENST00000437406.1:c.169G>A	ENSP00000403319.1:p.Ala57Thr
ENST00000451363.5:c.244G>A	ENSP00000414661.1:p.Ala82Thr
ENST00000464550.5:n.439G>A
ENST00000471657.1:n.406G>A
ENST00000481757.5:n.2537G>A
ENST00000486058.5:n.1716G>A
ENST00000493398.5:n.749G>A
NM_018226.4:c.1603G>A	NP_060696.4:p.Ala535Thr
XM_005247036.3:c.1570G>A	XP_005247093.1:p.Ala524Thr
NM_018226.5:c.1603G>A	NP_060696.4:p.Ala535Thr
XM_005247036.4:c.1570G>A	XP_005247093.1:p.Ala524Thr
NM_018226.6:c.1603G>A MANE Select	NP_060696.4:p.Ala535Thr