Canonical Allele Identifier: CA2321403959
Gene: RAB11B HGNC NCBI
ELAVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404420C= , CM000681.2:g.8404420C= GRCh38
NC_000019.9:g.8469304C= , CM000681.1:g.8469304C= GRCh37
NC_000019.8:g.8375304C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328024.11:c.*862C= (RAB11B) MANE Select ENSP00000333547.5:n.*862C=
ENST00000328024.10:c.*862C= (RAB11B) ENSP00000333547.5:n.*862C=
ENST00000351593.9:c.-88+40586G= (ELAVL1) ENSP00000264073.6:n.-88+40586G=
NM_004218.3:c.*862C= (RAB11B) NP_004209.2:n.*862C=
NM_004218.4:c.*862C= (RAB11B) MANE Select NP_004209.2:n.*862C=