Canonical Allele Identifier: CA351285986

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241515991C>A (hg19) ; chr2:g.240576574C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576574C>A , CM000664.2:g.240576574C>A	GRCh38
NC_000002.11:g.241515991C>A , CM000664.1:g.241515991C>A	GRCh37
NC_000002.10:g.241164664C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1550C>A MANE Select	ENSP00000270357.4:p.Pro517Gln
ENST00000270357.8:c.857C>A	ENSP00000270357.3:p.Pro286Gln
ENST00000437406.1:c.116C>A	ENSP00000403319.1:p.Pro39Gln
ENST00000451363.5:c.191C>A	ENSP00000414661.1:p.Pro64Gln
ENST00000464550.5:n.386C>A
ENST00000471657.1:n.353C>A
ENST00000481757.5:n.2484C>A
ENST00000486058.5:n.1663C>A
ENST00000493398.5:n.696C>A
NM_018226.4:c.1550C>A	NP_060696.4:p.Pro517Gln
XM_005247036.3:c.1517C>A	XP_005247093.1:p.Pro506Gln
NM_018226.5:c.1550C>A	NP_060696.4:p.Pro517Gln
XM_005247036.4:c.1517C>A	XP_005247093.1:p.Pro506Gln
NM_018226.6:c.1550C>A MANE Select	NP_060696.4:p.Pro517Gln