Canonical Allele Identifier: CA1339183974
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576616G= , CM000664.2:g.240576616G= GRCh38
NC_000002.11:g.241516033G= , CM000664.1:g.241516033G= GRCh37
NC_000002.10:g.241164706G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1592G= MANE Select ENSP00000270357.4:p.Arg531=
ENST00000270357.8:c.899G= ENSP00000270357.3:p.Arg300=
ENST00000437406.1:c.158G= ENSP00000403319.1:p.Arg53=
ENST00000451363.5:c.233G= ENSP00000414661.1:p.Arg78=
ENST00000464550.5:n.428G=
ENST00000471657.1:n.395G=
ENST00000481757.5:n.2526G=
ENST00000486058.5:n.1705G=
ENST00000493398.5:n.738G=
NM_018226.4:c.1592G= NP_060696.4:p.Arg531=
XM_005247036.3:c.1559G= XP_005247093.1:p.Arg520=
NM_018226.5:c.1592G= NP_060696.4:p.Arg531=
XM_005247036.4:c.1559G= XP_005247093.1:p.Arg520=
NM_018226.6:c.1592G= MANE Select NP_060696.4:p.Arg531=