Canonical Allele Identifier: CA432232461
Gene: RNPEPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241516037C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240576620C>A , CM000664.2:g.240576620C>A GRCh38
NC_000002.11:g.241516037C>A , CM000664.1:g.241516037C>A GRCh37
NC_000002.10:g.241164710C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270357.10:c.1596C>A MANE Select ENSP00000270357.4:p.Pro532=
ENST00000270357.8:c.903C>A ENSP00000270357.3:p.Pro301=
ENST00000437406.1:c.162C>A ENSP00000403319.1:p.Pro54=
ENST00000451363.5:c.237C>A ENSP00000414661.1:p.Pro79=
ENST00000464550.5:n.432C>A
ENST00000471657.1:n.399C>A
ENST00000481757.5:n.2530C>A
ENST00000486058.5:n.1709C>A
ENST00000493398.5:n.742C>A
NM_018226.4:c.1596C>A NP_060696.4:p.Pro532=
XM_005247036.3:c.1563C>A XP_005247093.1:p.Pro521=
NM_018226.5:c.1596C>A NP_060696.4:p.Pro532=
XM_005247036.4:c.1563C>A XP_005247093.1:p.Pro521=
NM_018226.6:c.1596C>A MANE Select NP_060696.4:p.Pro532=