Canonical Allele Identifier: CA1339183954
Gene: RNPEPL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576570C= , CM000664.2:g.240576570C= GRCh38
NC_000002.11:g.241515987C= , CM000664.1:g.241515987C= GRCh37
NC_000002.10:g.241164660C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1546C= MANE Select ENSP00000270357.4:p.Pro516=
ENST00000270357.8:c.853C= ENSP00000270357.3:p.Pro285=
ENST00000437406.1:c.112C= ENSP00000403319.1:p.Pro38=
ENST00000451363.5:c.187C= ENSP00000414661.1:p.Pro63=
ENST00000464550.5:n.382C=
ENST00000471657.1:n.349C=
ENST00000481757.5:n.2480C=
ENST00000486058.5:n.1659C=
ENST00000493398.5:n.692C=
NM_018226.4:c.1546C= NP_060696.4:p.Pro516=
XM_005247036.3:c.1513C= XP_005247093.1:p.Pro505=
NM_018226.5:c.1546C= NP_060696.4:p.Pro516=
XM_005247036.4:c.1513C= XP_005247093.1:p.Pro505=
NM_018226.6:c.1546C= MANE Select NP_060696.4:p.Pro516=