Canonical Allele Identifier: CA2321403960
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404422_8404423delinsTC , CM000681.2:g.8404422_8404423delinsTC GRCh38
NC_000019.9:g.8469306_8469307delinsTC , CM000681.1:g.8469306_8469307delinsTC GRCh37
NC_000019.8:g.8375306_8375307delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*864_*865delinsTC (RAB11B) MANE Select ENSP00000333547.5:n.*864_*865delinsTC
ENST00000328024.10:c.*864_*865delinsTC (RAB11B) ENSP00000333547.5:n.*864_*865delinsTC
ENST00000351593.9:c.-88+40583_-88+40584delinsGA (ELAVL1) ENSP00000264073.6:n.-88+40583_-88+40584delinsGA
NM_004218.3:c.*864_*865delinsTC (RAB11B) NP_004209.2:n.*864_*865delinsTC
NM_004218.4:c.*864_*865delinsTC (RAB11B) MANE Select NP_004209.2:n.*864_*865delinsTC