Canonical Allele Identifier: CA3246278216

Gene: MOV10L1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50092027G= , CM000684.2:g.50092027G=	GRCh38
NC_000022.10:g.50530456G= , CM000684.1:g.50530456G=	GRCh37
NC_000022.9:g.48872583G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018995.3:c.124G= MANE Select	NP_061868.1:p.Gly42=
ENST00000262794.10:c.124G= MANE Select	ENSP00000262794.5:p.Gly42=
NM_001164104.1:c.124G=	NP_001157576.1:p.Gly42=
NM_001164104.2:c.124G=	NP_001157576.1:p.Gly42=
NM_001164105.1:c.64G=	NP_001157577.1:p.Gly22=
NM_001164105.2:c.64G=	NP_001157577.1:p.Gly22=
NM_018995.2:c.124G=	NP_061868.1:p.Gly42=
ENST00000262794.9:c.124G=	ENSP00000262794.5:p.Gly42=
ENST00000395854.6:c.*280G=	ENSP00000379195.2:n.*280G=
ENST00000395858.7:c.124G=	ENSP00000379199.3:p.Gly42=
ENST00000419054.5:c.*1230G=	ENSP00000410957.1:n.*1230G=
ENST00000475190.1:n.169G=
ENST00000540615.5:c.64G=	ENSP00000438542.1:p.Gly22=
ENST00000545383.5:c.124G=	ENSP00000438978.1:p.Gly42=
XM_005261923.2:c.64G=	XP_005261980.1:p.Gly22=
XM_005261923.4:c.64G=	XP_005261980.1:p.Gly22=
XM_011530696.1:c.124G=	XP_011528998.1:p.Gly42=
XM_011530697.1:c.64G=	XP_011528999.1:p.Gly22=
XM_011530698.1:c.124G=	XP_011529000.1:p.Gly42=
XM_011530699.1:c.-33G=	XP_011529001.1:n.-33G=
XM_011530700.1:c.-33G=	XP_011529002.1:n.-33G=
XM_011530700.2:c.-33G=	XP_011529002.1:n.-33G=
XM_011530701.1:c.124G=	XP_011529003.1:p.Gly42=
XM_011530702.1:c.-440G=	XP_011529004.1:n.-440G=
XM_011530704.1:c.124G=	XP_011529006.1:p.Gly42=
XM_017028833.1:c.124G=	XP_016884322.1:p.Gly42=
XM_017028834.1:c.124G=	XP_016884323.1:p.Gly42=
XM_017028837.1:c.124G=	XP_016884326.1:p.Gly42=
XR_002958704.1:n.207G=
XR_430479.1:n.207G=