Canonical Allele Identifier: CA392919977

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65877395A>C , CM000677.2:g.65877395A>C	GRCh38
NC_000015.9:g.66169733A>C , CM000677.1:g.66169733A>C	GRCh37
NC_000015.8:g.63956787A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004663.5:c.104A>C MANE Select	NP_004654.1:p.Glu35Ala
ENST00000261890.7:c.104A>C MANE Select	ENSP00000261890.2:p.Glu35Ala
NM_001206836.1:c.104A>C	NP_001193765.1:p.Glu35Ala
NM_001206836.2:c.104A>C	NP_001193765.1:p.Glu35Ala
NM_004663.4:c.104A>C	NP_004654.1:p.Glu35Ala
ENST00000261890.6:c.104A>C	ENSP00000261890.2:p.Glu35Ala
ENST00000564910.5:c.76+28A>C	ENSP00000455567.1:n.76+28A>C
ENST00000565075.5:c.104A>C	ENSP00000456638.1:p.Glu35Ala
ENST00000566233.5:c.104A>C	ENSP00000454381.1:p.Glu35Ala
ENST00000567671.1:c.-254A>C	ENSP00000454673.1:n.-254A>C
ENST00000568850.5:n.361A>C
ENST00000569304.1:n.125-10306A>C
ENST00000569896.1:c.104A>C	ENSP00000456420.1:p.Glu35Ala