Canonical Allele Identifier: CA351286088

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516020T>A (hg19) ; chr2:g.240576603T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576603T>A , CM000664.2:g.240576603T>A	GRCh38
NC_000002.11:g.241516020T>A , CM000664.1:g.241516020T>A	GRCh37
NC_000002.10:g.241164693T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1579T>A MANE Select	ENSP00000270357.4:p.Ser527Thr
ENST00000270357.8:c.886T>A	ENSP00000270357.3:p.Ser296Thr
ENST00000437406.1:c.145T>A	ENSP00000403319.1:p.Ser49Thr
ENST00000451363.5:c.220T>A	ENSP00000414661.1:p.Ser74Thr
ENST00000464550.5:n.415T>A
ENST00000471657.1:n.382T>A
ENST00000481757.5:n.2513T>A
ENST00000486058.5:n.1692T>A
ENST00000493398.5:n.725T>A
NM_018226.4:c.1579T>A	NP_060696.4:p.Ser527Thr
XM_005247036.3:c.1546T>A	XP_005247093.1:p.Ser516Thr
NM_018226.5:c.1579T>A	NP_060696.4:p.Ser527Thr
XM_005247036.4:c.1546T>A	XP_005247093.1:p.Ser516Thr
NM_018226.6:c.1579T>A MANE Select	NP_060696.4:p.Ser527Thr