Canonical Allele Identifier: CA1881759918
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522948A= , CM000671.2:g.131522948A= GRCh38
NC_000009.11:g.134398335A= , CM000671.1:g.134398335A= GRCh37
NC_000009.10:g.133388156A= NCBI36
NG_008896.1:g.25047A=
NG_008896.2:g.25047A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1858A= ENSP00000343034.7:p.Ser620=
ENST00000404875.7:n.2560A=
ENST00000423007.6:c.2077A= ENSP00000404119.2:p.Ser693=
ENST00000677295.2:c.*2364A= ENSP00000504346.2:n.*2364A=
ENST00000678264.2:c.*2203A= ENSP00000503157.2:n.*2203A=
ENST00000682070.1:n.2330A=
ENST00000682639.1:c.17A=
ENST00000682813.1:n.2417A=
ENST00000683231.1:c.17A=
ENST00000683392.1:n.4612A=
ENST00000683712.1:n.2425A=
ENST00000683900.1:n.3920A=
ENST00000684062.1:n.2686A=
ENST00000684399.1:c.17A=
ENST00000684579.1:n.3866A=
ENST00000341012.12:c.1858A= ENSP00000343034.7:p.Ser620=
ENST00000372220.5:c.889A= ENSP00000361294.5:p.Ser297=
ENST00000372228.9:c.2086A= ENSP00000361302.3:p.Ser696=
ENST00000402686.8:c.2020A= MANE Select ENSP00000385797.4:p.Ser674=
ENST00000676640.1:c.2020A= ENSP00000503281.1:p.Ser674=
ENST00000676803.1:c.1081A= ENSP00000503093.1:p.Ser361=
ENST00000676835.1:c.*1235A= ENSP00000502911.1:n.*1235A=
ENST00000677029.1:c.1564A= ENSP00000502936.1:p.Ser522=
ENST00000677099.1:c.*1730A= ENSP00000504553.1:n.*1730A=
ENST00000677216.1:c.1669A= ENSP00000503772.1:p.Ser557=
ENST00000677221.1:n.1045A=
ENST00000677295.1:c.*1242A= ENSP00000504346.1:n.*1242A=
ENST00000677444.1:c.1965A=
ENST00000677586.1:n.1387A=
ENST00000677626.1:c.1669A= ENSP00000503552.1:p.Ser557=
ENST00000677853.1:c.*1028A= ENSP00000503488.1:n.*1028A=
ENST00000678264.1:c.*1397A= ENSP00000503157.1:n.*1397A=
ENST00000678303.1:c.1930A= ENSP00000503696.1:p.Ser644=
ENST00000678366.1:c.*2269A= ENSP00000504353.1:n.*2269A=
ENST00000678546.1:c.*1965A= ENSP00000503062.1:n.*1965A=
ENST00000678548.1:c.*2159A= ENSP00000503934.1:n.*2159A=
ENST00000678626.1:n.1856A=
ENST00000678739.1:c.*2186A= ENSP00000503806.1:n.*2186A=
ENST00000678833.1:c.*1772A= ENSP00000503893.1:n.*1772A=
ENST00000679023.1:c.1858A= ENSP00000503718.1:p.Ser620=
ENST00000679076.1:c.1639A=
ENST00000679111.1:c.*776A= ENSP00000504257.1:n.*776A=
ENST00000679189.1:c.1669A= ENSP00000503356.1:p.Ser557=
ENST00000341012.11:c.1858A= ENSP00000343034.7:p.Ser620=
ENST00000372220.4:c.883A= ENSP00000361294.4:p.Ser295=
ENST00000372228.7:c.2086A= ENSP00000361302.3:p.Ser696=
ENST00000402686.7:c.2020A= ENSP00000385797.3:p.Ser674=
ENST00000404875.6:c.1669A= ENSP00000384531.2:p.Ser557=
ENST00000423007.5:c.2020A= ENSP00000404119.1:p.Ser674=
ENST00000485278.5:n.2570A=
NM_001077365.1:c.2020A= NP_001070833.1:p.Ser674=
NM_001077366.1:c.1858A= NP_001070834.1:p.Ser620=
NM_001136113.1:c.2020A= NP_001129585.1:p.Ser674=
NM_001136114.1:c.1669A= NP_001129586.1:p.Ser557=
NM_007171.3:c.2086A= NP_009102.3:p.Ser696=
XM_005272156.1:c.2086A= XP_005272213.1:p.Ser696=
XM_005272158.1:c.1924A= XP_005272215.1:p.Ser642=
XM_005272159.1:c.1735A= XP_005272216.1:p.Ser579=
XM_005272162.1:c.889A= XP_005272219.1:p.Ser297=
XM_006716932.1:c.1735A= XP_006716995.1:p.Ser579=
XM_011518140.1:c.1939A= XP_011516442.1:p.Ser647=
XM_011518141.1:c.1873A= XP_011516443.1:p.Ser625=
XM_011518142.1:c.1777A= XP_011516444.1:p.Ser593=
XM_011518143.1:c.1771A= XP_011516445.1:p.Ser591=
XM_011518145.1:c.1630A= XP_011516447.1:p.Ser544=
XM_011518147.1:c.958A= XP_011516449.1:p.Ser320=
XR_929703.1:n.2262A=
NM_001353193.1:c.2086A= NP_001340122.1:p.Ser696=
NM_001353194.1:c.1858A= NP_001340123.1:p.Ser620=
NM_001353195.1:c.1669A= NP_001340124.1:p.Ser557=
NM_001353196.1:c.1930A= NP_001340125.1:p.Ser644=
NM_001353197.1:c.1924A= NP_001340126.1:p.Ser642=
NM_001353198.1:c.1924A= NP_001340127.1:p.Ser642=
NM_001353199.1:c.1735A= NP_001340128.1:p.Ser579=
NM_001353200.1:c.1564A= NP_001340129.1:p.Ser522=
NR_148391.1:n.2070A=
NR_148392.1:n.2288A=
NR_148393.1:n.2209A=
NR_148394.1:n.1963A=
NR_148395.1:n.2361A=
NR_148396.1:n.1995A=
NR_148397.1:n.2120A=
NR_148398.1:n.2075A=
NR_148399.1:n.2601A=
NR_148400.1:n.2200A=
XM_005272162.3:c.889A= XP_005272219.1:p.Ser297=
XM_006716932.2:c.1735A= XP_006716995.1:p.Ser579=
XM_011518140.2:c.1939A= XP_011516442.1:p.Ser647=
XM_011518141.2:c.1873A= XP_011516443.1:p.Ser625=
XM_011518142.2:c.1777A= XP_011516444.1:p.Ser593=
XM_011518143.2:c.1771A= XP_011516445.1:p.Ser591=
XM_011518145.2:c.1630A= XP_011516447.1:p.Ser544=
XM_017014205.2:c.889A= XP_016869694.1:p.Ser297=
XM_024447380.1:c.889A= XP_024303148.1:p.Ser297=
XM_024447381.1:c.1195A= XP_024303149.1:p.Ser399=
XM_024447382.1:c.889A= XP_024303150.1:p.Ser297=
XR_001746160.2:n.2190A=
XR_001746162.2:n.2395A=
XR_001746164.1:n.2112A=
XR_001746166.2:n.2407A=
NM_001077365.2:c.2020A= MANE Select NP_001070833.1:p.Ser674=
NM_001077366.2:c.1858A= NP_001070834.1:p.Ser620=
NM_001136113.2:c.2020A= NP_001129585.1:p.Ser674=
NM_001136114.2:c.1669A= NP_001129586.1:p.Ser557=
NM_001353193.2:c.2086A= NP_001340122.2:p.Ser696=
NM_001353194.2:c.1858A= NP_001340123.1:p.Ser620=
NM_001353195.2:c.1669A= NP_001340124.1:p.Ser557=
NM_001353196.2:c.1930A= NP_001340125.1:p.Ser644=
NM_001353197.2:c.1924A= NP_001340126.2:p.Ser642=
NM_001353198.2:c.1924A= NP_001340127.2:p.Ser642=
NM_001353199.2:c.1735A= NP_001340128.2:p.Ser579=
NM_001353200.2:c.1564A= NP_001340129.1:p.Ser522=
NM_001374689.1:c.2008A= NP_001361618.1:p.Ser670=
NM_001374690.1:c.1801A= NP_001361619.1:p.Ser601=
NM_001374691.1:c.1669A= NP_001361620.1:p.Ser557=
NM_001374692.1:c.1669A= NP_001361621.1:p.Ser557=
NM_001374693.1:c.1669A= NP_001361622.1:p.Ser557=
NM_001374695.1:c.1630A= NP_001361624.1:p.Ser544=
NM_007171.4:c.2086A= NP_009102.4:p.Ser696=
NR_148391.2:n.2054A=
NR_148392.2:n.2272A=
NR_148393.2:n.2193A=
NR_148394.2:n.1947A=
NR_148395.2:n.2345A=
NR_148396.2:n.1979A=
NR_148397.2:n.2104A=
NR_148398.2:n.2059A=
NR_148399.2:n.2585A=
NR_148400.2:n.2184A=