Canonical Allele Identifier: CA11440185

Gene: OSBPL10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.31754078C>T , CM000665.2:g.31754078C>T	GRCh38
NC_000003.11:g.31795570C>T , CM000665.1:g.31795570C>T	GRCh37
NC_000003.10:g.31770574C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698199.1:c.730-5958G>A	ENSP00000513603.1:n.730-5958G>A
ENST00000396556.7:c.730-5958G>A MANE Select	ENSP00000379804.2:n.730-5958G>A
ENST00000673388.1:c.118-5958G>A	ENSP00000500118.1:n.118-5958G>A
ENST00000396556.6:c.730-5958G>A	ENSP00000379804.2:n.730-5958G>A
ENST00000428241.1:c.154-5958G>A	ENSP00000399200.1:n.154-5958G>A
ENST00000429492.6:c.36-5958G>A
ENST00000438237.6:c.538-5958G>A	ENSP00000406124.2:n.538-5958G>A
ENST00000467647.1:n.142-5958G>A
ENST00000467955.5:n.563-5958G>A
ENST00000480671.5:n.305-5958G>A
ENST00000485205.5:n.422-5958G>A
NM_001174060.1:c.538-5958G>A	NP_001167531.1:n.538-5958G>A
NM_017784.4:c.730-5958G>A	NP_060254.2:n.730-5958G>A
XM_005264843.3:c.730-5958G>A	XP_005264900.1:n.730-5958G>A
XM_005264844.3:c.538-5958G>A	XP_005264901.1:n.538-5958G>A
XM_011533323.1:c.817-5958G>A	XP_011531625.1:n.817-5958G>A
XM_011533324.1:c.817-5958G>A	XP_011531626.1:n.817-5958G>A
XM_011533325.1:c.406-5958G>A	XP_011531627.1:n.406-5958G>A
XM_011533326.1:c.319-5958G>A	XP_011531628.1:n.319-5958G>A
XM_005264843.4:c.730-5958G>A	XP_005264900.1:n.730-5958G>A
XM_005264844.5:c.538-5958G>A	XP_005264901.1:n.538-5958G>A
XM_011533326.2:c.319-5958G>A	XP_011531628.1:n.319-5958G>A
XM_017005670.2:c.76-5958G>A	XP_016861159.1:n.76-5958G>A
NM_001174060.2:c.538-5958G>A	NP_001167531.1:n.538-5958G>A
NM_017784.5:c.730-5958G>A MANE Select	NP_060254.2:n.730-5958G>A