Canonical Allele Identifier: CA490845347

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65879696A>G , CM000677.2:g.65879696A>G	GRCh38
NC_000015.9:g.66172034A>G , CM000677.1:g.66172034A>G	GRCh37
NC_000015.8:g.63959088A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004663.5:c.456A>G MANE Select	NP_004654.1:p.Glu152=
ENST00000261890.7:c.456A>G MANE Select	ENSP00000261890.2:p.Glu152=
NM_001206836.1:c.439+17A>G	NP_001193765.1:n.439+17A>G
NM_001206836.2:c.439+17A>G	NP_001193765.1:n.439+17A>G
NM_004663.4:c.456A>G	NP_004654.1:p.Glu152=
ENST00000261890.6:c.456A>G	ENSP00000261890.2:p.Glu152=
ENST00000564910.5:c.246A>G	ENSP00000455567.1:p.Glu82=
ENST00000565075.5:c.431-29A>G	ENSP00000456638.1:n.431-29A>G
ENST00000566233.5:c.430+1741A>G	ENSP00000454381.1:n.430+1741A>G
ENST00000567671.1:c.99A>G	ENSP00000454673.1:p.Glu33=
ENST00000569304.1:n.125-8005A>G
ENST00000569896.1:c.439+17A>G	ENSP00000456420.1:n.439+17A>G