Canonical Allele Identifier: CA1881758391
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522222C= , CM000671.2:g.131522222C= GRCh38
NC_000009.11:g.134397609C= , CM000671.1:g.134397609C= GRCh37
NC_000009.10:g.133387430C= NCBI36
NG_008896.1:g.24321C=
NG_008896.2:g.24321C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1839C= ENSP00000343034.7:p.Cys613=
ENST00000404875.7:n.2541C=
ENST00000423007.6:c.2058C= ENSP00000404119.2:p.Cys686=
ENST00000677295.2:c.*2345C= ENSP00000504346.2:n.*2345C=
ENST00000678264.2:c.*2184C= ENSP00000503157.2:n.*2184C=
ENST00000682070.1:n.2311C=
ENST00000682813.1:n.2405C=
ENST00000683392.1:n.4593C=
ENST00000683712.1:n.2406C=
ENST00000683900.1:n.3901C=
ENST00000684062.1:n.2667C=
ENST00000684579.1:n.3847C=
ENST00000341012.12:c.1839C= ENSP00000343034.7:p.Cys613=
ENST00000372220.5:c.870C= ENSP00000361294.5:p.Cys290=
ENST00000372228.9:c.2067C= ENSP00000361302.3:p.Cys689=
ENST00000402686.8:c.2001C= MANE Select ENSP00000385797.4:p.Cys667=
ENST00000676640.1:c.2001C= ENSP00000503281.1:p.Cys667=
ENST00000676803.1:c.1062C= ENSP00000503093.1:p.Cys354=
ENST00000676835.1:c.*1216C= ENSP00000502911.1:n.*1216C=
ENST00000677029.1:c.1545C= ENSP00000502936.1:p.Cys515=
ENST00000677099.1:c.*1711C= ENSP00000504553.1:n.*1711C=
ENST00000677216.1:c.1650C= ENSP00000503772.1:p.Cys550=
ENST00000677221.1:n.1026C=
ENST00000677295.1:c.*1223C= ENSP00000504346.1:n.*1223C=
ENST00000677444.1:c.1946C=
ENST00000677586.1:n.1368C=
ENST00000677626.1:c.1650C= ENSP00000503552.1:p.Cys550=
ENST00000677853.1:c.*1009C= ENSP00000503488.1:n.*1009C=
ENST00000678264.1:c.*1378C= ENSP00000503157.1:n.*1378C=
ENST00000678303.1:c.1911C= ENSP00000503696.1:p.Cys637=
ENST00000678366.1:c.*2250C= ENSP00000504353.1:n.*2250C=
ENST00000678546.1:c.*1946C= ENSP00000503062.1:n.*1946C=
ENST00000678548.1:c.*2140C= ENSP00000503934.1:n.*2140C=
ENST00000678626.1:n.1837C=
ENST00000678739.1:c.*2167C= ENSP00000503806.1:n.*2167C=
ENST00000678833.1:c.*1753C= ENSP00000503893.1:n.*1753C=
ENST00000679023.1:c.1839C= ENSP00000503718.1:p.Cys613=
ENST00000679076.1:c.1620C=
ENST00000679111.1:c.*757C= ENSP00000504257.1:n.*757C=
ENST00000679189.1:c.1650C= ENSP00000503356.1:p.Cys550=
ENST00000341012.11:c.1839C= ENSP00000343034.7:p.Cys613=
ENST00000372220.4:c.864C= ENSP00000361294.4:p.Cys288=
ENST00000372228.7:c.2067C= ENSP00000361302.3:p.Cys689=
ENST00000402686.7:c.2001C= ENSP00000385797.3:p.Cys667=
ENST00000404875.6:c.1650C= ENSP00000384531.2:p.Cys550=
ENST00000423007.5:c.2001C= ENSP00000404119.1:p.Cys667=
ENST00000485278.5:n.2551C=
ENST00000494883.1:n.544C=
NM_001077365.1:c.2001C= NP_001070833.1:p.Cys667=
NM_001077366.1:c.1839C= NP_001070834.1:p.Cys613=
NM_001136113.1:c.2001C= NP_001129585.1:p.Cys667=
NM_001136114.1:c.1650C= NP_001129586.1:p.Cys550=
NM_007171.3:c.2067C= NP_009102.3:p.Cys689=
XM_005272156.1:c.2067C= XP_005272213.1:p.Cys689=
XM_005272158.1:c.1905C= XP_005272215.1:p.Cys635=
XM_005272159.1:c.1716C= XP_005272216.1:p.Cys572=
XM_005272162.1:c.870C= XP_005272219.1:p.Cys290=
XM_006716932.1:c.1716C= XP_006716995.1:p.Cys572=
XM_011518140.1:c.1920C= XP_011516442.1:p.Cys640=
XM_011518141.1:c.1854C= XP_011516443.1:p.Cys618=
XM_011518142.1:c.1758C= XP_011516444.1:p.Cys586=
XM_011518143.1:c.1752C= XP_011516445.1:p.Cys584=
XM_011518145.1:c.1611C= XP_011516447.1:p.Cys537=
XM_011518147.1:c.939C= XP_011516449.1:p.Cys313=
XR_929703.1:n.2243C=
NM_001353193.1:c.2067C= NP_001340122.1:p.Cys689=
NM_001353194.1:c.1839C= NP_001340123.1:p.Cys613=
NM_001353195.1:c.1650C= NP_001340124.1:p.Cys550=
NM_001353196.1:c.1911C= NP_001340125.1:p.Cys637=
NM_001353197.1:c.1905C= NP_001340126.1:p.Cys635=
NM_001353198.1:c.1905C= NP_001340127.1:p.Cys635=
NM_001353199.1:c.1716C= NP_001340128.1:p.Cys572=
NM_001353200.1:c.1545C= NP_001340129.1:p.Cys515=
NR_148391.1:n.2051C=
NR_148392.1:n.2269C=
NR_148393.1:n.2190C=
NR_148394.1:n.1944C=
NR_148395.1:n.2342C=
NR_148396.1:n.1976C=
NR_148397.1:n.2101C=
NR_148398.1:n.2056C=
NR_148399.1:n.2582C=
NR_148400.1:n.2181C=
XM_005272162.3:c.870C= XP_005272219.1:p.Cys290=
XM_006716932.2:c.1716C= XP_006716995.1:p.Cys572=
XM_011518140.2:c.1920C= XP_011516442.1:p.Cys640=
XM_011518141.2:c.1854C= XP_011516443.1:p.Cys618=
XM_011518142.2:c.1758C= XP_011516444.1:p.Cys586=
XM_011518143.2:c.1752C= XP_011516445.1:p.Cys584=
XM_011518145.2:c.1611C= XP_011516447.1:p.Cys537=
XM_017014205.2:c.870C= XP_016869694.1:p.Cys290=
XM_024447380.1:c.870C= XP_024303148.1:p.Cys290=
XM_024447381.1:c.1176C= XP_024303149.1:p.Cys392=
XM_024447382.1:c.870C= XP_024303150.1:p.Cys290=
XR_001746160.2:n.2171C=
XR_001746162.2:n.2376C=
XR_001746164.1:n.2093C=
XR_001746166.2:n.2388C=
NM_001077365.2:c.2001C= MANE Select NP_001070833.1:p.Cys667=
NM_001077366.2:c.1839C= NP_001070834.1:p.Cys613=
NM_001136113.2:c.2001C= NP_001129585.1:p.Cys667=
NM_001136114.2:c.1650C= NP_001129586.1:p.Cys550=
NM_001353193.2:c.2067C= NP_001340122.2:p.Cys689=
NM_001353194.2:c.1839C= NP_001340123.1:p.Cys613=
NM_001353195.2:c.1650C= NP_001340124.1:p.Cys550=
NM_001353196.2:c.1911C= NP_001340125.1:p.Cys637=
NM_001353197.2:c.1905C= NP_001340126.2:p.Cys635=
NM_001353198.2:c.1905C= NP_001340127.2:p.Cys635=
NM_001353199.2:c.1716C= NP_001340128.2:p.Cys572=
NM_001353200.2:c.1545C= NP_001340129.1:p.Cys515=
NM_001374689.1:c.1989C= NP_001361618.1:p.Cys663=
NM_001374690.1:c.1782C= NP_001361619.1:p.Cys594=
NM_001374691.1:c.1650C= NP_001361620.1:p.Cys550=
NM_001374692.1:c.1650C= NP_001361621.1:p.Cys550=
NM_001374693.1:c.1650C= NP_001361622.1:p.Cys550=
NM_001374695.1:c.1611C= NP_001361624.1:p.Cys537=
NM_007171.4:c.2067C= NP_009102.4:p.Cys689=
NR_148391.2:n.2035C=
NR_148392.2:n.2253C=
NR_148393.2:n.2174C=
NR_148394.2:n.1928C=
NR_148395.2:n.2326C=
NR_148396.2:n.1960C=
NR_148397.2:n.2085C=
NR_148398.2:n.2040C=
NR_148399.2:n.2566C=
NR_148400.2:n.2165C=