Canonical Allele Identifier: CA2663968553
Gene: RNPEPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576311_240576316dup , CM000664.2:g.240576311_240576316dup GRCh38
NC_000002.11:g.241515728_241515733dup , CM000664.1:g.241515728_241515733dup GRCh37
NC_000002.10:g.241164401_241164406dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-224_1511-219dup MANE Select ENSP00000270357.4:n.1511-224_1511-219dup
ENST00000270357.8:c.818-224_818-219dup ENSP00000270357.3:n.818-224_818-219dup
ENST00000437406.1:c.110-257_110-252dup ENSP00000403319.1:n.110-257_110-252dup
ENST00000451363.5:c.152-224_152-219dup ENSP00000414661.1:n.152-224_152-219dup
ENST00000464550.5:n.347-224_347-219dup
ENST00000471657.1:n.314-224_314-219dup
ENST00000481757.5:n.2221_2226dup
ENST00000486058.5:n.1624-224_1624-219dup
ENST00000493398.5:n.657-224_657-219dup
NM_018226.4:c.1511-224_1511-219dup NP_060696.4:n.1511-224_1511-219dup
XM_005247036.3:c.1511-257_1511-252dup XP_005247093.1:n.1511-257_1511-252dup
NM_018226.5:c.1511-224_1511-219dup NP_060696.4:n.1511-224_1511-219dup
XM_005247036.4:c.1511-257_1511-252dup XP_005247093.1:n.1511-257_1511-252dup
NM_018226.6:c.1511-224_1511-219dup MANE Select NP_060696.4:n.1511-224_1511-219dup