Canonical Allele Identifier: CA1009448
Gene: MOV10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112689033T>C , CM000663.2:g.112689033T>C GRCh38
NC_000001.10:g.113231655T>C , CM000663.1:g.113231655T>C GRCh37
NC_000001.9:g.113033178T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369645.6:c.236T>C MANE Select ENSP00000358659.1:p.Leu79Pro
ENST00000685268.1:n.159T>C
ENST00000686097.1:c.68T>C ENSP00000510374.1:p.Leu23Pro
ENST00000686428.1:c.236T>C ENSP00000508727.1:p.Leu79Pro
ENST00000686923.1:c.68T>C ENSP00000509824.1:p.Leu23Pro
ENST00000687509.1:n.237T>C
ENST00000689955.1:n.159T>C
ENST00000690243.1:n.336T>C
ENST00000357443.2:c.236T>C ENSP00000350028.2:p.Leu79Pro
ENST00000369644.5:c.68T>C ENSP00000358658.1:p.Leu23Pro
ENST00000369645.5:c.236T>C ENSP00000358659.1:p.Leu79Pro
ENST00000413052.6:c.236T>C ENSP00000399797.2:p.Leu79Pro
ENST00000468624.5:n.327T>C
ENST00000475429.5:n.450T>C
ENST00000496577.5:n.1073T>C
NM_001130079.2:c.236T>C NP_001123551.1:p.Leu79Pro
NM_001286072.1:c.68T>C NP_001273001.1:p.Leu23Pro
NM_020963.4:c.236T>C NP_066014.1:p.Leu79Pro
XM_005270868.3:c.236T>C XP_005270925.1:p.Leu79Pro
XM_005270869.3:c.68T>C XP_005270926.1:p.Leu23Pro
XM_005270870.3:c.68T>C XP_005270927.1:p.Leu23Pro
XM_006710644.2:c.236T>C XP_006710707.1:p.Leu79Pro
XR_426609.2:n.1293T>C
XR_946657.1:n.360T>C
NM_001321324.1:c.236T>C NP_001308253.1:p.Leu79Pro
XM_005270869.4:c.68T>C XP_005270926.1:p.Leu23Pro
XM_005270870.5:c.68T>C XP_005270927.1:p.Leu23Pro
XM_017001318.2:c.68T>C XP_016856807.1:p.Leu23Pro
XM_017001319.2:c.236T>C XP_016856808.1:p.Leu79Pro
XM_024447132.1:c.236T>C XP_024302900.1:p.Leu79Pro
XM_024447137.1:c.236T>C XP_024302905.1:p.Leu79Pro
XR_001737185.2:n.352T>C
XR_001737186.2:n.352T>C
XR_001737187.2:n.352T>C
XR_946657.2:n.352T>C
NM_001369507.1:c.236T>C NP_001356436.1:p.Leu79Pro
NM_001130079.3:c.236T>C NP_001123551.1:p.Leu79Pro
NM_001286072.2:c.68T>C NP_001273001.1:p.Leu23Pro
NM_001321324.2:c.236T>C MANE Select NP_001308253.1:p.Leu79Pro
NM_001389562.1:c.68T>C NP_001376491.1:p.Leu23Pro
NM_001389563.1:c.68T>C NP_001376492.1:p.Leu23Pro
NM_020963.5:c.236T>C NP_066014.1:p.Leu79Pro