Canonical Allele Identifier: CA2321403970
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Linked Data

dbSNP Id: rs1971464881
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404434del , CM000681.2:g.8404434del GRCh38
NC_000019.9:g.8469318del , CM000681.1:g.8469318del GRCh37
NC_000019.8:g.8375318del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*876del (RAB11B) MANE Select ENSP00000333547.5:n.*876del
ENST00000328024.10:c.*876del (RAB11B) ENSP00000333547.5:n.*876del
ENST00000351593.9:c.-88+40574del (ELAVL1) ENSP00000264073.6:n.-88+40574del
NM_004218.3:c.*876del (RAB11B) NP_004209.2:n.*876del
NM_004218.4:c.*876del (RAB11B) MANE Select NP_004209.2:n.*876del
Search 100 bp 5'
Search 100 bp 3'