Canonical Allele Identifier: CA392921689

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65877860A>G , CM000677.2:g.65877860A>G	GRCh38
NC_000015.9:g.66170198A>G , CM000677.1:g.66170198A>G	GRCh37
NC_000015.8:g.63957252A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261890.7:c.335A>G MANE Select	ENSP00000261890.2:p.His112Arg
ENST00000261890.6:c.335A>G	ENSP00000261890.2:p.His112Arg
ENST00000564910.5:c.125A>G	ENSP00000455567.1:p.His42Arg
ENST00000565075.5:c.335A>G	ENSP00000456638.1:p.His112Arg
ENST00000566233.5:c.335A>G	ENSP00000454381.1:p.His112Arg
ENST00000567671.1:c.-23A>G	ENSP00000454673.1:n.-23A>G
ENST00000569304.1:n.125-9841A>G
ENST00000569896.1:c.335A>G	ENSP00000456420.1:p.His112Arg
NM_001206836.1:c.335A>G	NP_001193765.1:p.His112Arg
NM_004663.4:c.335A>G	NP_004654.1:p.His112Arg
NM_004663.5:c.335A>G MANE Select	NP_004654.1:p.His112Arg
NM_001206836.2:c.335A>G	NP_001193765.1:p.His112Arg