Canonical Allele Identifier: CA351286337

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516070A>C (hg19) ; chr2:g.240576653A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576653A>C , CM000664.2:g.240576653A>C	GRCh38
NC_000002.11:g.241516070A>C , CM000664.1:g.241516070A>C	GRCh37
NC_000002.10:g.241164743A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1629A>C MANE Select	ENSP00000270357.4:p.Glu543Asp
ENST00000270357.8:c.936A>C	ENSP00000270357.3:p.Glu312Asp
ENST00000437406.1:c.195A>C	ENSP00000403319.1:p.Glu65Asp
ENST00000451363.5:c.270A>C	ENSP00000414661.1:p.Glu90Asp
ENST00000464550.5:n.465A>C
ENST00000471657.1:n.432A>C
ENST00000481757.5:n.2563A>C
ENST00000486058.5:n.1742A>C
ENST00000493398.5:n.775A>C
NM_018226.4:c.1629A>C	NP_060696.4:p.Glu543Asp
XM_005247036.3:c.1596A>C	XP_005247093.1:p.Glu532Asp
NM_018226.5:c.1629A>C	NP_060696.4:p.Glu543Asp
XM_005247036.4:c.1596A>C	XP_005247093.1:p.Glu532Asp
NM_018226.6:c.1629A>C MANE Select	NP_060696.4:p.Glu543Asp