Canonical Allele Identifier: CA1009462

Gene: MOV10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.112689081T>C , CM000663.2:g.112689081T>C	GRCh38
NC_000001.10:g.113231703T>C , CM000663.1:g.113231703T>C	GRCh37
NC_000001.9:g.113033226T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001321324.2:c.284T>C MANE Select	NP_001308253.1:p.Leu95Pro
ENST00000369645.6:c.284T>C MANE Select	ENSP00000358659.1:p.Leu95Pro
NM_001130079.2:c.284T>C	NP_001123551.1:p.Leu95Pro
NM_001130079.3:c.284T>C	NP_001123551.1:p.Leu95Pro
NM_001286072.1:c.116T>C	NP_001273001.1:p.Leu39Pro
NM_001286072.2:c.116T>C	NP_001273001.1:p.Leu39Pro
NM_001321324.1:c.284T>C	NP_001308253.1:p.Leu95Pro
NM_001369507.1:c.284T>C	NP_001356436.1:p.Leu95Pro
NM_001389562.1:c.116T>C	NP_001376491.1:p.Leu39Pro
NM_001389563.1:c.116T>C	NP_001376492.1:p.Leu39Pro
NM_020963.4:c.284T>C	NP_066014.1:p.Leu95Pro
NM_020963.5:c.284T>C	NP_066014.1:p.Leu95Pro
ENST00000357443.2:c.284T>C	ENSP00000350028.2:p.Leu95Pro
ENST00000369644.5:c.116T>C	ENSP00000358658.1:p.Leu39Pro
ENST00000369645.5:c.284T>C	ENSP00000358659.1:p.Leu95Pro
ENST00000413052.6:c.284T>C	ENSP00000399797.2:p.Leu95Pro
ENST00000468624.5:n.375T>C
ENST00000475429.5:n.498T>C
ENST00000496577.5:n.1121T>C
ENST00000685268.1:n.207T>C
ENST00000686097.1:c.116T>C	ENSP00000510374.1:p.Leu39Pro
ENST00000686428.1:c.284T>C	ENSP00000508727.1:p.Leu95Pro
ENST00000686923.1:c.116T>C	ENSP00000509824.1:p.Leu39Pro
ENST00000687509.1:n.285T>C
ENST00000689955.1:n.207T>C
ENST00000690243.1:n.384T>C
XM_005270868.3:c.284T>C	XP_005270925.1:p.Leu95Pro
XM_005270869.3:c.116T>C	XP_005270926.1:p.Leu39Pro
XM_005270869.4:c.116T>C	XP_005270926.1:p.Leu39Pro
XM_005270870.3:c.116T>C	XP_005270927.1:p.Leu39Pro
XM_005270870.5:c.116T>C	XP_005270927.1:p.Leu39Pro
XM_006710644.2:c.284T>C	XP_006710707.1:p.Leu95Pro
XM_017001318.2:c.116T>C	XP_016856807.1:p.Leu39Pro
XM_017001319.2:c.284T>C	XP_016856808.1:p.Leu95Pro
XM_024447132.1:c.284T>C	XP_024302900.1:p.Leu95Pro
XM_024447137.1:c.284T>C	XP_024302905.1:p.Leu95Pro
XR_001737185.2:n.400T>C
XR_001737186.2:n.400T>C
XR_001737187.2:n.400T>C
XR_426609.2:n.1341T>C
XR_946657.1:n.408T>C
XR_946657.2:n.400T>C