Canonical Allele Identifier: CA399002768

Gene: RAB11FIP4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31517725C>G , CM000679.2:g.31517725C>G	GRCh38
NC_000017.10:g.29844743C>G , CM000679.1:g.29844743C>G	GRCh37
NC_000017.9:g.26868863C>G	NCBI36
NG_051977.1:g.131102C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032932.6:c.411C>G MANE Select	NP_116321.2:p.Asp137Glu
ENST00000621161.5:c.411C>G MANE Select	ENSP00000482620.1:p.Asp137Glu
NM_001303542.2:c.105C>G	NP_001290471.2:p.Asp35Glu
NM_001303542.3:c.105C>G	NP_001290471.2:p.Asp35Glu
NM_001346747.1:c.105C>G	NP_001333676.1:p.Asp35Glu
NM_001346747.2:c.105C>G	NP_001333676.1:p.Asp35Glu
NM_001346748.1:c.-13C>G	NP_001333677.1:n.-13C>G
NM_001346748.2:c.-13C>G	NP_001333677.1:n.-13C>G
NM_001346749.1:c.-22-4190C>G	NP_001333678.1:n.-22-4190C>G
NM_001346749.2:c.-22-4190C>G	NP_001333678.1:n.-22-4190C>G
NM_032932.5:c.411C>G	NP_116321.2:p.Asp137Glu
ENST00000394744.6:c.105C>G	ENSP00000378227.2:p.Asp35Glu
ENST00000578694.1:c.*112C>G	ENSP00000463616.1:n.*112C>G
ENST00000582009.5:c.279C>G	ENSP00000463206.1:p.Asp93Glu
ENST00000583755.1:c.-22-4190C>G	ENSP00000465929.1:n.-22-4190C>G
ENST00000621161.4:c.411C>G	ENSP00000482620.1:p.Asp137Glu