Canonical Allele Identifier: CA1339183981
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576636C= , CM000664.2:g.240576636C= GRCh38
NC_000002.11:g.241516053C= , CM000664.1:g.241516053C= GRCh37
NC_000002.10:g.241164726C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1612C= MANE Select ENSP00000270357.4:p.Gln538=
ENST00000270357.8:c.919C= ENSP00000270357.3:p.Gln307=
ENST00000437406.1:c.178C= ENSP00000403319.1:p.Gln60=
ENST00000451363.5:c.253C= ENSP00000414661.1:p.Gln85=
ENST00000464550.5:n.448C=
ENST00000471657.1:n.415C=
ENST00000481757.5:n.2546C=
ENST00000486058.5:n.1725C=
ENST00000493398.5:n.758C=
NM_018226.4:c.1612C= NP_060696.4:p.Gln538=
XM_005247036.3:c.1579C= XP_005247093.1:p.Gln527=
NM_018226.5:c.1612C= NP_060696.4:p.Gln538=
XM_005247036.4:c.1579C= XP_005247093.1:p.Gln527=
NM_018226.6:c.1612C= MANE Select NP_060696.4:p.Gln538=