Canonical Allele Identifier: CA2663967198
Gene: RNPEPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576088A>T , CM000664.2:g.240576088A>T GRCh38
NC_000002.11:g.241515505A>T , CM000664.1:g.241515505A>T GRCh37
NC_000002.10:g.241164178A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-447A>T MANE Select ENSP00000270357.4:n.1511-447A>T
ENST00000270357.8:c.818-447A>T ENSP00000270357.3:n.818-447A>T
ENST00000437406.1:c.109+478A>T ENSP00000403319.1:n.109+478A>T
ENST00000451363.5:c.152-447A>T ENSP00000414661.1:n.152-447A>T
ENST00000464550.5:n.347-447A>T
ENST00000471657.1:n.314-447A>T
ENST00000481757.5:n.1998A>T
ENST00000486058.5:n.1624-447A>T
ENST00000493398.5:n.657-447A>T
NM_018226.4:c.1511-447A>T NP_060696.4:n.1511-447A>T
XM_005247036.3:c.1510+478A>T XP_005247093.1:n.1510+478A>T
NM_018226.5:c.1511-447A>T NP_060696.4:n.1511-447A>T
XM_005247036.4:c.1510+478A>T XP_005247093.1:n.1510+478A>T
NM_018226.6:c.1511-447A>T MANE Select NP_060696.4:n.1511-447A>T