Canonical Allele Identifier: CA7621574
Gene: RAB11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.65877807T>A , CM000677.2:g.65877807T>A GRCh38
NC_000015.9:g.66170145T>A , CM000677.1:g.66170145T>A GRCh37
NC_000015.8:g.63957199T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_004663.5:c.282T>A MANE Select NP_004654.1:p.Ala94=
ENST00000261890.7:c.282T>A MANE Select ENSP00000261890.2:p.Ala94=
NM_001206836.1:c.282T>A NP_001193765.1:p.Ala94=
NM_001206836.2:c.282T>A NP_001193765.1:p.Ala94=
NM_004663.4:c.282T>A NP_004654.1:p.Ala94=
ENST00000261890.6:c.282T>A ENSP00000261890.2:p.Ala94=
ENST00000564910.5:c.77-5T>A ENSP00000455567.1:n.77-5T>A
ENST00000565075.5:c.282T>A ENSP00000456638.1:p.Ala94=
ENST00000566233.5:c.282T>A ENSP00000454381.1:p.Ala94=
ENST00000567671.1:c.-76T>A ENSP00000454673.1:n.-76T>A
ENST00000568850.5:n.539T>A
ENST00000569304.1:n.125-9894T>A
ENST00000569896.1:c.282T>A ENSP00000456420.1:p.Ala94=