Canonical Allele Identifier: CA1881756647
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131521410A= , CM000671.2:g.131521410A= GRCh38
NC_000009.11:g.134396797A= , CM000671.1:g.134396797A= GRCh37
NC_000009.10:g.133386618A= NCBI36
NG_008896.1:g.23509A=
NG_008896.2:g.23509A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1601A= ENSP00000343034.7:p.Tyr534=
ENST00000404875.7:n.2303A=
ENST00000423007.6:c.1820A= ENSP00000404119.2:p.Tyr607=
ENST00000677295.2:c.*2107A= ENSP00000504346.2:n.*2107A=
ENST00000678264.2:c.*1946A= ENSP00000503157.2:n.*1946A=
ENST00000682070.1:n.2228A=
ENST00000682813.1:n.2167A=
ENST00000683392.1:n.4510A=
ENST00000683712.1:n.2168A=
ENST00000683900.1:n.3663A=
ENST00000684062.1:n.2429A=
ENST00000684579.1:n.3609A=
ENST00000684679.1:n.990A=
ENST00000341012.12:c.1601A= ENSP00000343034.7:p.Tyr534=
ENST00000372220.5:c.632A= ENSP00000361294.5:p.Tyr211=
ENST00000372228.9:c.1829A= ENSP00000361302.3:p.Tyr610=
ENST00000402686.8:c.1763A= MANE Select ENSP00000385797.4:p.Tyr588=
ENST00000676640.1:c.1763A= ENSP00000503281.1:p.Tyr588=
ENST00000676803.1:c.824A= ENSP00000503093.1:p.Tyr275=
ENST00000676835.1:c.*978A= ENSP00000502911.1:n.*978A=
ENST00000677029.1:c.1307A= ENSP00000502936.1:p.Tyr436=
ENST00000677099.1:c.*1473A= ENSP00000504553.1:n.*1473A=
ENST00000677216.1:c.1412A= ENSP00000503772.1:p.Tyr471=
ENST00000677221.1:n.788A=
ENST00000677295.1:c.*1140A= ENSP00000504346.1:n.*1140A=
ENST00000677444.1:c.1708A=
ENST00000677586.1:n.1130A=
ENST00000677626.1:c.1412A= ENSP00000503552.1:p.Tyr471=
ENST00000677853.1:c.*771A= ENSP00000503488.1:n.*771A=
ENST00000678202.1:n.922A=
ENST00000678264.1:c.*1140A= ENSP00000503157.1:n.*1140A=
ENST00000678303.1:c.1673A= ENSP00000503696.1:p.Tyr558=
ENST00000678366.1:c.*2012A= ENSP00000504353.1:n.*2012A=
ENST00000678546.1:c.*1708A= ENSP00000503062.1:n.*1708A=
ENST00000678548.1:c.*1835A= ENSP00000503934.1:n.*1835A=
ENST00000678626.1:n.1599A=
ENST00000678739.1:c.*2084A= ENSP00000503806.1:n.*2084A=
ENST00000678833.1:c.*1515A= ENSP00000503893.1:n.*1515A=
ENST00000679023.1:c.1601A= ENSP00000503718.1:p.Tyr534=
ENST00000679076.1:c.1382A=
ENST00000679111.1:c.*519A= ENSP00000504257.1:n.*519A=
ENST00000679189.1:c.1412A= ENSP00000503356.1:p.Tyr471=
ENST00000341012.11:c.1601A= ENSP00000343034.7:p.Tyr534=
ENST00000372220.4:c.626A= ENSP00000361294.4:p.Tyr209=
ENST00000372228.7:c.1829A= ENSP00000361302.3:p.Tyr610=
ENST00000402686.7:c.1763A= ENSP00000385797.3:p.Tyr588=
ENST00000404875.6:c.1412A= ENSP00000384531.2:p.Tyr471=
ENST00000423007.5:c.1763A= ENSP00000404119.1:p.Tyr588=
ENST00000485278.5:n.2313A=
ENST00000494883.1:n.306A=
NM_001077365.1:c.1763A= NP_001070833.1:p.Tyr588=
NM_001077366.1:c.1601A= NP_001070834.1:p.Tyr534=
NM_001136113.1:c.1763A= NP_001129585.1:p.Tyr588=
NM_001136114.1:c.1412A= NP_001129586.1:p.Tyr471=
NM_007171.3:c.1829A= NP_009102.3:p.Tyr610=
XM_005272156.1:c.1829A= XP_005272213.1:p.Tyr610=
XM_005272158.1:c.1667A= XP_005272215.1:p.Tyr556=
XM_005272159.1:c.1478A= XP_005272216.1:p.Tyr493=
XM_005272162.1:c.632A= XP_005272219.1:p.Tyr211=
XM_006716932.1:c.1478A= XP_006716995.1:p.Tyr493=
XM_011518140.1:c.1682A= XP_011516442.1:p.Tyr561=
XM_011518141.1:c.1616A= XP_011516443.1:p.Tyr539=
XM_011518142.1:c.1520A= XP_011516444.1:p.Tyr507=
XM_011518143.1:c.1514A= XP_011516445.1:p.Tyr505=
XM_011518145.1:c.1373A= XP_011516447.1:p.Tyr458=
XM_011518147.1:c.701A= XP_011516449.1:p.Tyr234=
XR_929703.1:n.2005A=
NM_001353193.1:c.1829A= NP_001340122.1:p.Tyr610=
NM_001353194.1:c.1601A= NP_001340123.1:p.Tyr534=
NM_001353195.1:c.1412A= NP_001340124.1:p.Tyr471=
NM_001353196.1:c.1673A= NP_001340125.1:p.Tyr558=
NM_001353197.1:c.1667A= NP_001340126.1:p.Tyr556=
NM_001353198.1:c.1667A= NP_001340127.1:p.Tyr556=
NM_001353199.1:c.1478A= NP_001340128.1:p.Tyr493=
NM_001353200.1:c.1307A= NP_001340129.1:p.Tyr436=
NR_148391.1:n.1813A=
NR_148392.1:n.2031A=
NR_148393.1:n.1952A=
NR_148394.1:n.1706A=
NR_148395.1:n.2104A=
NR_148396.1:n.1738A=
NR_148397.1:n.1863A=
NR_148398.1:n.1818A=
NR_148399.1:n.2344A=
NR_148400.1:n.1943A=
XM_005272162.3:c.632A= XP_005272219.1:p.Tyr211=
XM_006716932.2:c.1478A= XP_006716995.1:p.Tyr493=
XM_011518140.2:c.1682A= XP_011516442.1:p.Tyr561=
XM_011518141.2:c.1616A= XP_011516443.1:p.Tyr539=
XM_011518142.2:c.1520A= XP_011516444.1:p.Tyr507=
XM_011518143.2:c.1514A= XP_011516445.1:p.Tyr505=
XM_011518145.2:c.1373A= XP_011516447.1:p.Tyr458=
XM_017014205.2:c.632A= XP_016869694.1:p.Tyr211=
XM_024447380.1:c.632A= XP_024303148.1:p.Tyr211=
XM_024447381.1:c.938A= XP_024303149.1:p.Tyr313=
XM_024447382.1:c.632A= XP_024303150.1:p.Tyr211=
XR_001746160.2:n.1933A=
XR_001746162.2:n.2138A=
XR_001746164.1:n.1855A=
XR_001746166.2:n.2150A=
NM_001077365.2:c.1763A= MANE Select NP_001070833.1:p.Tyr588=
NM_001077366.2:c.1601A= NP_001070834.1:p.Tyr534=
NM_001136113.2:c.1763A= NP_001129585.1:p.Tyr588=
NM_001136114.2:c.1412A= NP_001129586.1:p.Tyr471=
NM_001353193.2:c.1829A= NP_001340122.2:p.Tyr610=
NM_001353194.2:c.1601A= NP_001340123.1:p.Tyr534=
NM_001353195.2:c.1412A= NP_001340124.1:p.Tyr471=
NM_001353196.2:c.1673A= NP_001340125.1:p.Tyr558=
NM_001353197.2:c.1667A= NP_001340126.2:p.Tyr556=
NM_001353198.2:c.1667A= NP_001340127.2:p.Tyr556=
NM_001353199.2:c.1478A= NP_001340128.2:p.Tyr493=
NM_001353200.2:c.1307A= NP_001340129.1:p.Tyr436=
NM_001374689.1:c.1751A= NP_001361618.1:p.Tyr584=
NM_001374690.1:c.1544A= NP_001361619.1:p.Tyr515=
NM_001374691.1:c.1412A= NP_001361620.1:p.Tyr471=
NM_001374692.1:c.1412A= NP_001361621.1:p.Tyr471=
NM_001374693.1:c.1412A= NP_001361622.1:p.Tyr471=
NM_001374695.1:c.1373A= NP_001361624.1:p.Tyr458=
NM_007171.4:c.1829A= NP_009102.4:p.Tyr610=
NR_148391.2:n.1797A=
NR_148392.2:n.2015A=
NR_148393.2:n.1936A=
NR_148394.2:n.1690A=
NR_148395.2:n.2088A=
NR_148396.2:n.1722A=
NR_148397.2:n.1847A=
NR_148398.2:n.1802A=
NR_148399.2:n.2328A=
NR_148400.2:n.1927A=