Canonical Allele Identifier: CA392921661

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65877856G>A , CM000677.2:g.65877856G>A	GRCh38
NC_000015.9:g.66170194G>A , CM000677.1:g.66170194G>A	GRCh37
NC_000015.8:g.63957248G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004663.5:c.331G>A MANE Select	NP_004654.1:p.Asp111Asn
ENST00000261890.7:c.331G>A MANE Select	ENSP00000261890.2:p.Asp111Asn
NM_001206836.1:c.331G>A	NP_001193765.1:p.Asp111Asn
NM_001206836.2:c.331G>A	NP_001193765.1:p.Asp111Asn
NM_004663.4:c.331G>A	NP_004654.1:p.Asp111Asn
ENST00000261890.6:c.331G>A	ENSP00000261890.2:p.Asp111Asn
ENST00000564910.5:c.121G>A	ENSP00000455567.1:p.Asp41Asn
ENST00000565075.5:c.331G>A	ENSP00000456638.1:p.Asp111Asn
ENST00000566233.5:c.331G>A	ENSP00000454381.1:p.Asp111Asn
ENST00000567671.1:c.-27G>A	ENSP00000454673.1:n.-27G>A
ENST00000569304.1:n.125-9845G>A
ENST00000569896.1:c.331G>A	ENSP00000456420.1:p.Asp111Asn