Canonical Allele Identifier: CA1339183708
Gene: RNPEPL1 HGNC NCBI

Linked Data

dbSNP Id: rs2093036952

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576109C>A , CM000664.2:g.240576109C>A GRCh38
NC_000002.11:g.241515526C>A , CM000664.1:g.241515526C>A GRCh37
NC_000002.10:g.241164199C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270357.10:c.1511-426C>A MANE Select ENSP00000270357.4:n.1511-426C>A
ENST00000270357.8:c.818-426C>A ENSP00000270357.3:n.818-426C>A
ENST00000437406.1:c.110-459C>A ENSP00000403319.1:n.110-459C>A
ENST00000451363.5:c.152-426C>A ENSP00000414661.1:n.152-426C>A
ENST00000464550.5:n.347-426C>A
ENST00000471657.1:n.314-426C>A
ENST00000481757.5:n.2019C>A
ENST00000486058.5:n.1624-426C>A
ENST00000493398.5:n.657-426C>A
NM_018226.4:c.1511-426C>A NP_060696.4:n.1511-426C>A
XM_005247036.3:c.1511-459C>A XP_005247093.1:n.1511-459C>A
NM_018226.5:c.1511-426C>A NP_060696.4:n.1511-426C>A
XM_005247036.4:c.1511-459C>A XP_005247093.1:n.1511-459C>A
NM_018226.6:c.1511-426C>A MANE Select NP_060696.4:n.1511-426C>A