Canonical Allele Identifier: CA432232152
Gene: RNPEPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241516082G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576665G>A , CM000664.2:g.240576665G>A GRCh38
NC_000002.11:g.241516082G>A , CM000664.1:g.241516082G>A GRCh37
NC_000002.10:g.241164755G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1641G>A MANE Select ENSP00000270357.4:p.Gln547=
ENST00000270357.8:c.948G>A ENSP00000270357.3:p.Gln316=
ENST00000437406.1:c.207G>A ENSP00000403319.1:p.Gln69=
ENST00000451363.5:c.282G>A ENSP00000414661.1:p.Gln94=
ENST00000464550.5:n.477G>A
ENST00000471657.1:n.444G>A
ENST00000481757.5:n.2575G>A
ENST00000486058.5:n.1754G>A
ENST00000493398.5:n.787G>A
NM_018226.4:c.1641G>A NP_060696.4:p.Gln547=
XM_005247036.3:c.1608G>A XP_005247093.1:p.Gln536=
NM_018226.5:c.1641G>A NP_060696.4:p.Gln547=
XM_005247036.4:c.1608G>A XP_005247093.1:p.Gln536=
NM_018226.6:c.1641G>A MANE Select NP_060696.4:p.Gln547=