Canonical Allele Identifier: CA970888448
Gene: RAB11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65877318C>T , CM000677.2:g.65877318C>T GRCh38
NC_000015.9:g.66169656C>T , CM000677.1:g.66169656C>T GRCh37
NC_000015.8:g.63956710C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004663.5:c.41-14C>T MANE Select NP_004654.1:n.41-14C>T
ENST00000261890.7:c.41-14C>T MANE Select ENSP00000261890.2:n.41-14C>T
NM_001206836.1:c.41-14C>T NP_001193765.1:n.41-14C>T
NM_001206836.2:c.41-14C>T NP_001193765.1:n.41-14C>T
NM_004663.4:c.41-14C>T NP_004654.1:n.41-14C>T
ENST00000261890.6:c.41-14C>T ENSP00000261890.2:n.41-14C>T
ENST00000564910.5:c.41-14C>T ENSP00000455567.1:n.41-14C>T
ENST00000565075.5:c.41-14C>T ENSP00000456638.1:n.41-14C>T
ENST00000566233.5:c.41-14C>T ENSP00000454381.1:n.41-14C>T
ENST00000567671.1:c.-317-14C>T ENSP00000454673.1:n.-317-14C>T
ENST00000568850.5:n.298-14C>T
ENST00000569304.1:n.125-10383C>T
ENST00000569896.1:c.41-14C>T ENSP00000456420.1:n.41-14C>T