Canonical Allele Identifier: CA351286264

Gene: RNPEPL1

Linked Data

• dbSNP Id: rs2093038423
• MyVariant Identifiers: chr2:g.241516054A>G (hg19) ; chr2:g.240576637A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576637A>G , CM000664.2:g.240576637A>G	GRCh38
NC_000002.11:g.241516054A>G , CM000664.1:g.241516054A>G	GRCh37
NC_000002.10:g.241164727A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1613A>G MANE Select	ENSP00000270357.4:p.Gln538Arg
ENST00000270357.8:c.920A>G	ENSP00000270357.3:p.Gln307Arg
ENST00000437406.1:c.179A>G	ENSP00000403319.1:p.Gln60Arg
ENST00000451363.5:c.254A>G	ENSP00000414661.1:p.Gln85Arg
ENST00000464550.5:n.449A>G
ENST00000471657.1:n.416A>G
ENST00000481757.5:n.2547A>G
ENST00000486058.5:n.1726A>G
ENST00000493398.5:n.759A>G
NM_018226.4:c.1613A>G	NP_060696.4:p.Gln538Arg
XM_005247036.3:c.1580A>G	XP_005247093.1:p.Gln527Arg
NM_018226.5:c.1613A>G	NP_060696.4:p.Gln538Arg
XM_005247036.4:c.1580A>G	XP_005247093.1:p.Gln527Arg
NM_018226.6:c.1613A>G MANE Select	NP_060696.4:p.Gln538Arg