Canonical Allele Identifier: CA2211598613
Gene: VPS35L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.19583859_19583860delinsTC , CM000678.2:g.19583859_19583860delinsTC GRCh38
NC_000016.9:g.19595181_19595182delinsTC , CM000678.1:g.19595181_19595182delinsTC GRCh37
NC_000016.8:g.19502682_19502683delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000417362.7:c.639+2206_639+2207delinsTC MANE Select ENSP00000395973.3:n.639+2206_639+2207delinsTC
ENST00000251143.9:c.906+2206_906+2207delinsTC ENSP00000251143.6:n.906+2206_906+2207delinsTC
ENST00000417362.6:c.639+2206_639+2207delinsTC ENSP00000395973.3:n.639+2206_639+2207delinsTC
ENST00000438132.7:c.906+2206_906+2207delinsTC ENSP00000400815.3:n.906+2206_906+2207delinsTC
ENST00000448695.5:c.274+2205_274+2206delinsTC ENSP00000398009.2:n.274+2205_274+2206delinsTC
ENST00000513947.8:c.639+2206_639+2207delinsTC ENSP00000458116.3:n.639+2206_639+2207delinsTC
ENST00000539322.5:c.*139+2206_*139+2207delinsTC ENSP00000438852.1:n.*139+2206_*139+2207delinsTC
ENST00000542263.5:c.906+2206_906+2207delinsTC ENSP00000442468.1:n.906+2206_906+2207delinsTC
ENST00000543152.5:c.-30+2206_-30+2207delinsTC ENSP00000457973.1:n.-30+2206_-30+2207delinsTC
NM_001300743.1:c.906+2206_906+2207delinsTC NP_001287672.1:n.906+2206_906+2207delinsTC
NM_020314.5:c.906+2206_906+2207delinsTC NP_064710.4:n.906+2206_906+2207delinsTC
XM_005255435.2:c.906+2206_906+2207delinsTC XP_005255492.1:n.906+2206_906+2207delinsTC
XM_006721065.2:c.906+2206_906+2207delinsTC XP_006721128.1:n.906+2206_906+2207delinsTC
XM_011545895.1:c.906+2206_906+2207delinsTC XP_011544197.1:n.906+2206_906+2207delinsTC
XM_011545896.1:c.-321+2206_-321+2207delinsTC XP_011544198.1:n.-321+2206_-321+2207delinsTC
NM_001300743.2:c.639+2206_639+2207delinsTC NP_001287672.2:n.639+2206_639+2207delinsTC
NM_001365293.1:c.639+2206_639+2207delinsTC NP_001352222.1:n.639+2206_639+2207delinsTC
NM_001365294.1:c.639+2206_639+2207delinsTC NP_001352223.1:n.639+2206_639+2207delinsTC
NM_001365295.1:c.-321+2206_-321+2207delinsTC NP_001352224.1:n.-321+2206_-321+2207delinsTC
NM_020314.6:c.639+2206_639+2207delinsTC NP_064710.5:n.639+2206_639+2207delinsTC
NR_158160.1:n.666+2206_666+2207delinsTC
NR_158161.1:n.666+2206_666+2207delinsTC
NM_001300743.3:c.639+2206_639+2207delinsTC NP_001287672.2:n.639+2206_639+2207delinsTC
NM_001365293.2:c.639+2206_639+2207delinsTC NP_001352222.1:n.639+2206_639+2207delinsTC
NM_001365294.2:c.639+2206_639+2207delinsTC NP_001352223.1:n.639+2206_639+2207delinsTC
NM_001365295.2:c.-321+2206_-321+2207delinsTC NP_001352224.1:n.-321+2206_-321+2207delinsTC
NM_020314.7:c.639+2206_639+2207delinsTC MANE Select NP_064710.5:n.639+2206_639+2207delinsTC
NR_158160.2:n.666+2206_666+2207delinsTC
NR_158161.2:n.666+2206_666+2207delinsTC