Canonical Allele Identifier: CA2588087872
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404426_8404427del , CM000681.2:g.8404426_8404427del GRCh38
NC_000019.9:g.8469310_8469311del , CM000681.1:g.8469310_8469311del GRCh37
NC_000019.8:g.8375310_8375311del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*868_*869del (RAB11B) MANE Select ENSP00000333547.5:n.*868_*869del
ENST00000328024.10:c.*868_*869del (RAB11B) ENSP00000333547.5:n.*868_*869del
ENST00000351593.9:c.-88+40580_-88+40581del (ELAVL1) ENSP00000264073.6:n.-88+40580_-88+40581del
NM_004218.3:c.*868_*869del (RAB11B) NP_004209.2:n.*868_*869del
NM_004218.4:c.*868_*869del (RAB11B) MANE Select NP_004209.2:n.*868_*869del