Canonical Allele Identifier: CA351286260

Gene: RNPEPL1

Linked Data

• dbSNP Id: rs2093038417
• MyVariant Identifiers: chr2:g.241516053C>A (hg19) ; chr2:g.240576636C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576636C>A , CM000664.2:g.240576636C>A	GRCh38
NC_000002.11:g.241516053C>A , CM000664.1:g.241516053C>A	GRCh37
NC_000002.10:g.241164726C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1612C>A MANE Select	ENSP00000270357.4:p.Gln538Lys
ENST00000270357.8:c.919C>A	ENSP00000270357.3:p.Gln307Lys
ENST00000437406.1:c.178C>A	ENSP00000403319.1:p.Gln60Lys
ENST00000451363.5:c.253C>A	ENSP00000414661.1:p.Gln85Lys
ENST00000464550.5:n.448C>A
ENST00000471657.1:n.415C>A
ENST00000481757.5:n.2546C>A
ENST00000486058.5:n.1725C>A
ENST00000493398.5:n.758C>A
NM_018226.4:c.1612C>A	NP_060696.4:p.Gln538Lys
XM_005247036.3:c.1579C>A	XP_005247093.1:p.Gln527Lys
NM_018226.5:c.1612C>A	NP_060696.4:p.Gln538Lys
XM_005247036.4:c.1579C>A	XP_005247093.1:p.Gln527Lys
NM_018226.6:c.1612C>A MANE Select	NP_060696.4:p.Gln538Lys