Canonical Allele Identifier: CA10303832

Gene: MOV10L1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50092222G>A , CM000684.2:g.50092222G>A	GRCh38
NC_000022.10:g.50530651G>A , CM000684.1:g.50530651G>A	GRCh37
NC_000022.9:g.48872778G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262794.10:c.282+37G>A MANE Select	ENSP00000262794.5:n.282+37G>A
ENST00000262794.9:c.282+37G>A	ENSP00000262794.5:n.282+37G>A
ENST00000395854.6:c.*438+37G>A	ENSP00000379195.2:n.*438+37G>A
ENST00000395858.7:c.282+37G>A	ENSP00000379199.3:n.282+37G>A
ENST00000419054.5:c.*1388+37G>A	ENSP00000410957.1:n.*1388+37G>A
ENST00000475190.1:n.327+37G>A
ENST00000540615.5:c.222+37G>A	ENSP00000438542.1:n.222+37G>A
ENST00000545383.5:c.282+37G>A	ENSP00000438978.1:n.282+37G>A
NM_001164104.1:c.282+37G>A	NP_001157576.1:n.282+37G>A
NM_001164105.1:c.222+37G>A	NP_001157577.1:n.222+37G>A
NM_018995.2:c.282+37G>A	NP_061868.1:n.282+37G>A
XM_005261923.2:c.222+37G>A	XP_005261980.1:n.222+37G>A
XM_011530696.1:c.282+37G>A	XP_011528998.1:n.282+37G>A
XM_011530697.1:c.222+37G>A	XP_011528999.1:n.222+37G>A
XM_011530698.1:c.282+37G>A	XP_011529000.1:n.282+37G>A
XM_011530699.1:c.126+37G>A	XP_011529001.1:n.126+37G>A
XM_011530700.1:c.126+37G>A	XP_011529002.1:n.126+37G>A
XM_011530701.1:c.282+37G>A	XP_011529003.1:n.282+37G>A
XM_011530702.1:c.-282+37G>A	XP_011529004.1:n.-282+37G>A
XM_011530704.1:c.282+37G>A	XP_011529006.1:n.282+37G>A
XR_430479.1:n.365+37G>A
XM_005261923.4:c.222+37G>A	XP_005261980.1:n.222+37G>A
XM_011530700.2:c.126+37G>A	XP_011529002.1:n.126+37G>A
XM_017028833.1:c.282+37G>A	XP_016884322.1:n.282+37G>A
XM_017028834.1:c.282+37G>A	XP_016884323.1:n.282+37G>A
XM_017028837.1:c.282+37G>A	XP_016884326.1:n.282+37G>A
XR_002958704.1:n.365+37G>A
NM_018995.3:c.282+37G>A MANE Select	NP_061868.1:n.282+37G>A
NM_001164104.2:c.282+37G>A	NP_001157576.1:n.282+37G>A
NM_001164105.2:c.222+37G>A	NP_001157577.1:n.222+37G>A