Canonical Allele Identifier: CA351286389

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516079C>G (hg19) ; chr2:g.240576662C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576662C>G , CM000664.2:g.240576662C>G	GRCh38
NC_000002.11:g.241516079C>G , CM000664.1:g.241516079C>G	GRCh37
NC_000002.10:g.241164752C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1638C>G MANE Select	ENSP00000270357.4:p.Asp546Glu
ENST00000270357.8:c.945C>G	ENSP00000270357.3:p.Asp315Glu
ENST00000437406.1:c.204C>G	ENSP00000403319.1:p.Asp68Glu
ENST00000451363.5:c.279C>G	ENSP00000414661.1:p.Asp93Glu
ENST00000464550.5:n.474C>G
ENST00000471657.1:n.441C>G
ENST00000481757.5:n.2572C>G
ENST00000486058.5:n.1751C>G
ENST00000493398.5:n.784C>G
NM_018226.4:c.1638C>G	NP_060696.4:p.Asp546Glu
XM_005247036.3:c.1605C>G	XP_005247093.1:p.Asp535Glu
NM_018226.5:c.1638C>G	NP_060696.4:p.Asp546Glu
XM_005247036.4:c.1605C>G	XP_005247093.1:p.Asp535Glu
NM_018226.6:c.1638C>G MANE Select	NP_060696.4:p.Asp546Glu