Canonical Allele Identifier: CA11330590

Gene: OSBPL6

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178239571T>C , CM000664.2:g.178239571T>C	GRCh38
NC_000002.11:g.179104298T>C , CM000664.1:g.179104298T>C	GRCh37
NC_000002.10:g.178812544T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000190611.9:c.-351+44897T>C MANE Select	ENSP00000190611.4:n.-351+44897T>C
ENST00000190611.8:c.-351+44897T>C	ENSP00000190611.4:n.-351+44897T>C
ENST00000357080.8:c.-351+44897T>C	ENSP00000349591.4:n.-351+44897T>C
ENST00000359685.7:c.-351+44897T>C	ENSP00000352713.3:n.-351+44897T>C
ENST00000392505.6:c.-351+44897T>C	ENSP00000376293.2:n.-351+44897T>C
ENST00000409045.7:c.-351+44897T>C	ENSP00000387248.3:n.-351+44897T>C
ENST00000477646.1:n.274+9058T>C
NM_001201480.1:c.-351+44897T>C	NP_001188409.1:n.-351+44897T>C
NM_001201481.1:c.-351+44897T>C	NP_001188410.1:n.-351+44897T>C
NM_001201482.1:c.-351+44897T>C	NP_001188411.1:n.-351+44897T>C
NM_032523.3:c.-351+44897T>C	NP_115912.1:n.-351+44897T>C
XM_005246268.1:c.-351+44897T>C	XP_005246325.1:n.-351+44897T>C
XM_011510539.1:c.-351+44897T>C	XP_011508841.1:n.-351+44897T>C
XM_011510539.2:c.-351+44897T>C	XP_011508841.1:n.-351+44897T>C
XM_017003265.2:c.-361+44897T>C	XP_016858754.1:n.-361+44897T>C
XM_017003266.1:c.-351+9058T>C	XP_016858755.1:n.-351+9058T>C
XM_017003267.2:c.-312+44897T>C	XP_016858756.1:n.-312+44897T>C
XM_017003268.2:c.-351+44897T>C	XP_016858757.1:n.-351+44897T>C
XM_017003269.2:c.-312+44897T>C	XP_016858758.1:n.-312+44897T>C
XM_017003270.1:c.-351+22630T>C	XP_016858759.1:n.-351+22630T>C
XM_017003271.2:c.-312+44897T>C	XP_016858760.1:n.-312+44897T>C
XM_017003272.2:c.-351+44897T>C	XP_016858761.1:n.-351+44897T>C
XM_017003273.2:c.-351+44897T>C	XP_016858762.1:n.-351+44897T>C
XM_017003274.2:c.-351+44897T>C	XP_016858763.1:n.-351+44897T>C
XM_017003275.1:c.-351+9058T>C	XP_016858764.1:n.-351+9058T>C
XM_017003276.2:c.-351+44897T>C	XP_016858765.1:n.-351+44897T>C
XM_017003277.2:c.-351+44897T>C	XP_016858766.1:n.-351+44897T>C
XM_024452654.1:c.-1806+44897T>C	XP_024308422.1:n.-1806+44897T>C
XM_024452655.1:c.-1713+44897T>C	XP_024308423.1:n.-1713+44897T>C
NM_032523.4:c.-351+44897T>C MANE Select	NP_115912.1:n.-351+44897T>C
NM_001201480.2:c.-351+44897T>C	NP_001188409.1:n.-351+44897T>C
NM_001201481.2:c.-351+44897T>C	NP_001188410.1:n.-351+44897T>C
NM_001201482.2:c.-351+44897T>C	NP_001188411.1:n.-351+44897T>C