Canonical Allele Identifier: CA1339183837
Gene: RNPEPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1575438718

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576315A>C , CM000664.2:g.240576315A>C GRCh38
NC_000002.11:g.241515732A>C , CM000664.1:g.241515732A>C GRCh37
NC_000002.10:g.241164405A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1511-220A>C MANE Select ENSP00000270357.4:n.1511-220A>C
ENST00000270357.8:c.818-220A>C ENSP00000270357.3:n.818-220A>C
ENST00000437406.1:c.110-253A>C ENSP00000403319.1:n.110-253A>C
ENST00000451363.5:c.152-220A>C ENSP00000414661.1:n.152-220A>C
ENST00000464550.5:n.347-220A>C
ENST00000471657.1:n.314-220A>C
ENST00000481757.5:n.2225A>C
ENST00000486058.5:n.1624-220A>C
ENST00000493398.5:n.657-220A>C
NM_018226.4:c.1511-220A>C NP_060696.4:n.1511-220A>C
XM_005247036.3:c.1511-253A>C XP_005247093.1:n.1511-253A>C
NM_018226.5:c.1511-220A>C NP_060696.4:n.1511-220A>C
XM_005247036.4:c.1511-253A>C XP_005247093.1:n.1511-253A>C
NM_018226.6:c.1511-220A>C MANE Select NP_060696.4:n.1511-220A>C