Canonical Allele Identifier: CA2321403950
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404406A= , CM000681.2:g.8404406A= GRCh38
NC_000019.9:g.8469290A= , CM000681.1:g.8469290A= GRCh37
NC_000019.8:g.8375290A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*848A= (RAB11B) MANE Select ENSP00000333547.5:n.*848A=
ENST00000328024.10:c.*848A= (RAB11B) ENSP00000333547.5:n.*848A=
ENST00000351593.9:c.-88+40600T= (ELAVL1) ENSP00000264073.6:n.-88+40600T=
NM_004218.3:c.*848A= (RAB11B) NP_004209.2:n.*848A=
NM_004218.4:c.*848A= (RAB11B) MANE Select NP_004209.2:n.*848A=