Canonical Allele Identifier: CA2580089869

Gene: RAB11A

Linked Data

• ClinVar Variation Id: 2096048
• ClinVar RCV Id: RCV003013971

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65877759C>T , CM000677.2:g.65877759C>T	GRCh38
NC_000015.9:g.66170097C>T , CM000677.1:g.66170097C>T	GRCh37
NC_000015.8:g.63957151C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261890.7:c.237-3C>T MANE Select	ENSP00000261890.2:n.237-3C>T
ENST00000261890.6:c.237-3C>T	ENSP00000261890.2:n.237-3C>T
ENST00000564910.5:c.77-53C>T	ENSP00000455567.1:n.77-53C>T
ENST00000565075.5:c.237-3C>T	ENSP00000456638.1:n.237-3C>T
ENST00000566233.5:c.237-3C>T	ENSP00000454381.1:n.237-3C>T
ENST00000567671.1:c.-121-3C>T	ENSP00000454673.1:n.-121-3C>T
ENST00000568850.5:n.494-3C>T
ENST00000569304.1:n.125-9942C>T
ENST00000569896.1:c.237-3C>T	ENSP00000456420.1:n.237-3C>T
NM_001206836.1:c.237-3C>T	NP_001193765.1:n.237-3C>T
NM_004663.4:c.237-3C>T	NP_004654.1:n.237-3C>T
NM_004663.5:c.237-3C>T MANE Select	NP_004654.1:n.237-3C>T
NM_001206836.2:c.237-3C>T	NP_001193765.1:n.237-3C>T