Canonical Allele Identifier: CA16294821
Gene: OSBPL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24943836C>T , CM000669.2:g.24943836C>T GRCh38
NC_000007.13:g.24983455C>T , CM000669.1:g.24983455C>T GRCh37
NC_000007.12:g.24949980C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000313367.7:c.-150+36050G>A MANE Select ENSP00000315410.2:n.-150+36050G>A
ENST00000313367.6:c.-150+36050G>A ENSP00000315410.2:n.-150+36050G>A
ENST00000415952.1:c.-150+37563G>A ENSP00000411249.1:n.-150+37563G>A
NM_015550.3:c.-150+36050G>A NP_056365.1:n.-150+36050G>A
XM_006715681.2:c.-150+36050G>A XP_006715744.1:n.-150+36050G>A
XM_006715682.2:c.-150+36050G>A XP_006715745.1:n.-150+36050G>A
XM_006715683.2:c.-150+36050G>A XP_006715746.1:n.-150+36050G>A
XM_011515259.1:c.-629+36050G>A XP_011513561.1:n.-629+36050G>A
XR_428073.2:n.314+36050G>A
XR_428074.2:n.299+36050G>A
XR_428075.2:n.299+36050G>A
XR_926927.1:n.314+36050G>A
XR_926928.1:n.314+36050G>A
XR_926929.1:n.314+36050G>A
XM_006715681.3:c.-150+36050G>A XP_006715744.1:n.-150+36050G>A
XM_006715682.3:c.-150+36050G>A XP_006715745.1:n.-150+36050G>A
XM_006715683.3:c.-150+36050G>A XP_006715746.1:n.-150+36050G>A
XM_006715684.4:c.-1193+36050G>A XP_006715747.1:n.-1193+36050G>A
XM_011515259.2:c.-629+36050G>A XP_011513561.1:n.-629+36050G>A
XM_017011948.1:c.-492+36050G>A XP_016867437.1:n.-492+36050G>A
XM_017011949.1:c.-629+36050G>A XP_016867438.1:n.-629+36050G>A
XR_001744620.1:n.333+36050G>A
XR_428073.3:n.333+36050G>A
XR_428074.3:n.333+36050G>A
XR_428075.3:n.333+36050G>A
XR_926927.2:n.314+36050G>A
NM_015550.4:c.-150+36050G>A MANE Select NP_056365.1:n.-150+36050G>A