Canonical Allele Identifier: CA432232138

Gene: RNPEPL1

Linked Data

• MyVariant Identifiers: chr2:g.241516067A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240576650A>C , CM000664.2:g.240576650A>C	GRCh38
NC_000002.11:g.241516067A>C , CM000664.1:g.241516067A>C	GRCh37
NC_000002.10:g.241164740A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270357.10:c.1626A>C MANE Select	ENSP00000270357.4:p.Ala542=
ENST00000270357.8:c.933A>C	ENSP00000270357.3:p.Ala311=
ENST00000437406.1:c.192A>C	ENSP00000403319.1:p.Ala64=
ENST00000451363.5:c.267A>C	ENSP00000414661.1:p.Ala89=
ENST00000464550.5:n.462A>C
ENST00000471657.1:n.429A>C
ENST00000481757.5:n.2560A>C
ENST00000486058.5:n.1739A>C
ENST00000493398.5:n.772A>C
NM_018226.4:c.1626A>C	NP_060696.4:p.Ala542=
XM_005247036.3:c.1593A>C	XP_005247093.1:p.Ala531=
NM_018226.5:c.1626A>C	NP_060696.4:p.Ala542=
XM_005247036.4:c.1593A>C	XP_005247093.1:p.Ala531=
NM_018226.6:c.1626A>C MANE Select	NP_060696.4:p.Ala542=