Canonical Allele Identifier: CA490845191

Gene: RAB11A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65877888T>C , CM000677.2:g.65877888T>C	GRCh38
NC_000015.9:g.66170226T>C , CM000677.1:g.66170226T>C	GRCh37
NC_000015.8:g.63957280T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004663.5:c.363T>C MANE Select	NP_004654.1:p.Leu121=
ENST00000261890.7:c.363T>C MANE Select	ENSP00000261890.2:p.Leu121=
NM_001206836.1:c.363T>C	NP_001193765.1:p.Leu121=
NM_001206836.2:c.363T>C	NP_001193765.1:p.Leu121=
NM_004663.4:c.363T>C	NP_004654.1:p.Leu121=
ENST00000261890.6:c.363T>C	ENSP00000261890.2:p.Leu121=
ENST00000564910.5:c.153T>C	ENSP00000455567.1:p.Leu51=
ENST00000565075.5:c.363T>C	ENSP00000456638.1:p.Leu121=
ENST00000566233.5:c.363T>C	ENSP00000454381.1:p.Leu121=
ENST00000567671.1:c.6T>C	ENSP00000454673.1:p.Leu2=
ENST00000569304.1:n.125-9813T>C
ENST00000569896.1:c.363T>C	ENSP00000456420.1:p.Leu121=