Canonical Allele Identifier: CA271610659

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65869597C>A , CM000677.2:g.65869597C>A	GRCh38
NC_000015.9:g.66161935C>A , CM000677.1:g.66161935C>A	GRCh37
NC_000015.8:g.63948989C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261890.7:c.12C>A MANE Select	ENSP00000261890.2:p.Arg4=
ENST00000261890.6:c.12C>A	ENSP00000261890.2:p.Arg4=
ENST00000564910.5:c.12C>A	ENSP00000455567.1:p.Arg4=
ENST00000565075.5:c.12C>A	ENSP00000456638.1:p.Arg4=
ENST00000566233.5:c.12C>A	ENSP00000454381.1:p.Arg4=
ENST00000568850.5:n.298-7735C>A
ENST00000569304.1:n.125-18104C>A
ENST00000569896.1:c.12C>A	ENSP00000456420.1:p.Arg4=
NM_001206836.1:c.12C>A	NP_001193765.1:p.Arg4=
NM_004663.4:c.12C>A	NP_004654.1:p.Arg4=
NM_004663.5:c.12C>A MANE Select	NP_004654.1:p.Arg4=
NM_001206836.2:c.12C>A	NP_001193765.1:p.Arg4=