Canonical Allele Identifier: CA2697549156

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65877959A>G , CM000677.2:g.65877959A>G	GRCh38
NC_000015.9:g.66170297A>G , CM000677.1:g.66170297A>G	GRCh37
NC_000015.8:g.63957351A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261890.7:c.430+4A>G MANE Select	ENSP00000261890.2:n.430+4A>G
ENST00000261890.6:c.430+4A>G	ENSP00000261890.2:n.430+4A>G
ENST00000564910.5:c.220+4A>G	ENSP00000455567.1:n.220+4A>G
ENST00000565075.5:c.430+4A>G	ENSP00000456638.1:n.430+4A>G
ENST00000566233.5:c.430+4A>G	ENSP00000454381.1:n.430+4A>G
ENST00000567671.1:c.73+4A>G	ENSP00000454673.1:n.73+4A>G
ENST00000569304.1:n.125-9742A>G
ENST00000569896.1:c.430+4A>G	ENSP00000456420.1:n.430+4A>G
NM_001206836.1:c.430+4A>G	NP_001193765.1:n.430+4A>G
NM_004663.4:c.430+4A>G	NP_004654.1:n.430+4A>G
NM_004663.5:c.430+4A>G MANE Select	NP_004654.1:n.430+4A>G
NM_001206836.2:c.430+4A>G	NP_001193765.1:n.430+4A>G