Canonical Allele Identifier: CA392923433

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65879740C>A , CM000677.2:g.65879740C>A	GRCh38
NC_000015.9:g.66172078C>A , CM000677.1:g.66172078C>A	GRCh37
NC_000015.8:g.63959132C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004663.5:c.500C>A MANE Select	NP_004654.1:p.Thr167Lys
ENST00000261890.7:c.500C>A MANE Select	ENSP00000261890.2:p.Thr167Lys
NM_001206836.1:c.439+61C>A	NP_001193765.1:n.439+61C>A
NM_001206836.2:c.439+61C>A	NP_001193765.1:n.439+61C>A
NM_004663.4:c.500C>A	NP_004654.1:p.Thr167Lys
ENST00000261890.6:c.500C>A	ENSP00000261890.2:p.Thr167Lys
ENST00000564910.5:c.290C>A	ENSP00000455567.1:p.Thr97Lys
ENST00000565075.5:c.446C>A	ENSP00000456638.1:p.Thr149Lys
ENST00000566233.5:c.430+1785C>A	ENSP00000454381.1:n.430+1785C>A
ENST00000567671.1:c.143C>A	ENSP00000454673.1:p.Thr48Lys
ENST00000569304.1:n.125-7961C>A
ENST00000569896.1:c.439+61C>A	ENSP00000456420.1:n.439+61C>A