Canonical Allele Identifier: CA2692219277
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131521506T>G , CM000671.2:g.131521506T>G GRCh38
NC_000009.11:g.134396893T>G , CM000671.1:g.134396893T>G GRCh37
NC_000009.10:g.133386714T>G NCBI36
NG_008896.1:g.23605T>G
NG_008896.2:g.23605T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1663+34T>G ENSP00000343034.7:n.1663+34T>G
ENST00000404875.7:n.2365+34T>G
ENST00000423007.6:c.1882+34T>G ENSP00000404119.2:n.1882+34T>G
ENST00000677295.2:c.*2169+34T>G ENSP00000504346.2:n.*2169+34T>G
ENST00000678264.2:c.*2008+34T>G ENSP00000503157.2:n.*2008+34T>G
ENST00000682070.1:n.2290+34T>G
ENST00000682813.1:n.2229+34T>G
ENST00000683392.1:n.4572+34T>G
ENST00000683712.1:n.2230+34T>G
ENST00000683900.1:n.3725+34T>G
ENST00000684062.1:n.2491+34T>G
ENST00000684579.1:n.3671+34T>G
ENST00000684679.1:n.1052+34T>G
ENST00000341012.12:c.1663+34T>G ENSP00000343034.7:n.1663+34T>G
ENST00000372220.5:c.694+34T>G ENSP00000361294.5:n.694+34T>G
ENST00000372228.9:c.1891+34T>G ENSP00000361302.3:n.1891+34T>G
ENST00000402686.8:c.1825+34T>G MANE Select ENSP00000385797.4:n.1825+34T>G
ENST00000676640.1:c.1825+34T>G ENSP00000503281.1:n.1825+34T>G
ENST00000676803.1:c.886+34T>G ENSP00000503093.1:n.886+34T>G
ENST00000676835.1:c.*1040+34T>G ENSP00000502911.1:n.*1040+34T>G
ENST00000677029.1:c.1369+34T>G ENSP00000502936.1:n.1369+34T>G
ENST00000677099.1:c.*1535+34T>G ENSP00000504553.1:n.*1535+34T>G
ENST00000677216.1:c.1474+34T>G ENSP00000503772.1:n.1474+34T>G
ENST00000677221.1:n.850+34T>G
ENST00000677295.1:c.*1202+34T>G ENSP00000504346.1:n.*1202+34T>G
ENST00000677444.1:c.1770+34T>G
ENST00000677586.1:n.1192+34T>G
ENST00000677626.1:c.1474+34T>G ENSP00000503552.1:n.1474+34T>G
ENST00000677853.1:c.*833+34T>G ENSP00000503488.1:n.*833+34T>G
ENST00000678202.1:n.984+34T>G
ENST00000678264.1:c.*1202+34T>G ENSP00000503157.1:n.*1202+34T>G
ENST00000678303.1:c.1735+34T>G ENSP00000503696.1:n.1735+34T>G
ENST00000678366.1:c.*2074+34T>G ENSP00000504353.1:n.*2074+34T>G
ENST00000678546.1:c.*1770+34T>G ENSP00000503062.1:n.*1770+34T>G
ENST00000678548.1:c.*1897+34T>G ENSP00000503934.1:n.*1897+34T>G
ENST00000678626.1:n.1661+34T>G
ENST00000678739.1:c.*2146+34T>G ENSP00000503806.1:n.*2146+34T>G
ENST00000678833.1:c.*1577+34T>G ENSP00000503893.1:n.*1577+34T>G
ENST00000679023.1:c.1663+34T>G ENSP00000503718.1:n.1663+34T>G
ENST00000679076.1:c.1444+34T>G
ENST00000679111.1:c.*581+34T>G ENSP00000504257.1:n.*581+34T>G
ENST00000679189.1:c.1474+34T>G ENSP00000503356.1:n.1474+34T>G
ENST00000341012.11:c.1663+34T>G ENSP00000343034.7:n.1663+34T>G
ENST00000372220.4:c.688+34T>G ENSP00000361294.4:n.688+34T>G
ENST00000372228.7:c.1891+34T>G ENSP00000361302.3:n.1891+34T>G
ENST00000402686.7:c.1825+34T>G ENSP00000385797.3:n.1825+34T>G
ENST00000404875.6:c.1474+34T>G ENSP00000384531.2:n.1474+34T>G
ENST00000423007.5:c.1825+34T>G ENSP00000404119.1:n.1825+34T>G
ENST00000485278.5:n.2375+34T>G
ENST00000494883.1:n.368+34T>G
NM_001077365.1:c.1825+34T>G NP_001070833.1:n.1825+34T>G
NM_001077366.1:c.1663+34T>G NP_001070834.1:n.1663+34T>G
NM_001136113.1:c.1825+34T>G NP_001129585.1:n.1825+34T>G
NM_001136114.1:c.1474+34T>G NP_001129586.1:n.1474+34T>G
NM_007171.3:c.1891+34T>G NP_009102.3:n.1891+34T>G
XM_005272156.1:c.1891+34T>G XP_005272213.1:n.1891+34T>G
XM_005272158.1:c.1729+34T>G XP_005272215.1:n.1729+34T>G
XM_005272159.1:c.1540+34T>G XP_005272216.1:n.1540+34T>G
XM_005272162.1:c.694+34T>G XP_005272219.1:n.694+34T>G
XM_006716932.1:c.1540+34T>G XP_006716995.1:n.1540+34T>G
XM_011518140.1:c.1744+34T>G XP_011516442.1:n.1744+34T>G
XM_011518141.1:c.1678+34T>G XP_011516443.1:n.1678+34T>G
XM_011518142.1:c.1582+34T>G XP_011516444.1:n.1582+34T>G
XM_011518143.1:c.1576+34T>G XP_011516445.1:n.1576+34T>G
XM_011518145.1:c.1435+34T>G XP_011516447.1:n.1435+34T>G
XM_011518147.1:c.763+34T>G XP_011516449.1:n.763+34T>G
XR_929703.1:n.2067+34T>G
NM_001353193.1:c.1891+34T>G NP_001340122.1:n.1891+34T>G
NM_001353194.1:c.1663+34T>G NP_001340123.1:n.1663+34T>G
NM_001353195.1:c.1474+34T>G NP_001340124.1:n.1474+34T>G
NM_001353196.1:c.1735+34T>G NP_001340125.1:n.1735+34T>G
NM_001353197.1:c.1729+34T>G NP_001340126.1:n.1729+34T>G
NM_001353198.1:c.1729+34T>G NP_001340127.1:n.1729+34T>G
NM_001353199.1:c.1540+34T>G NP_001340128.1:n.1540+34T>G
NM_001353200.1:c.1369+34T>G NP_001340129.1:n.1369+34T>G
NR_148391.1:n.1875+34T>G
NR_148392.1:n.2093+34T>G
NR_148393.1:n.2014+34T>G
NR_148394.1:n.1768+34T>G
NR_148395.1:n.2166+34T>G
NR_148396.1:n.1800+34T>G
NR_148397.1:n.1925+34T>G
NR_148398.1:n.1880+34T>G
NR_148399.1:n.2406+34T>G
NR_148400.1:n.2005+34T>G
XM_005272162.3:c.694+34T>G XP_005272219.1:n.694+34T>G
XM_006716932.2:c.1540+34T>G XP_006716995.1:n.1540+34T>G
XM_011518140.2:c.1744+34T>G XP_011516442.1:n.1744+34T>G
XM_011518141.2:c.1678+34T>G XP_011516443.1:n.1678+34T>G
XM_011518142.2:c.1582+34T>G XP_011516444.1:n.1582+34T>G
XM_011518143.2:c.1576+34T>G XP_011516445.1:n.1576+34T>G
XM_011518145.2:c.1435+34T>G XP_011516447.1:n.1435+34T>G
XM_017014205.2:c.694+34T>G XP_016869694.1:n.694+34T>G
XM_024447380.1:c.694+34T>G XP_024303148.1:n.694+34T>G
XM_024447381.1:c.1000+34T>G XP_024303149.1:n.1000+34T>G
XM_024447382.1:c.694+34T>G XP_024303150.1:n.694+34T>G
XR_001746160.2:n.1995+34T>G
XR_001746162.2:n.2200+34T>G
XR_001746164.1:n.1917+34T>G
XR_001746166.2:n.2212+34T>G
NM_001077365.2:c.1825+34T>G MANE Select NP_001070833.1:n.1825+34T>G
NM_001077366.2:c.1663+34T>G NP_001070834.1:n.1663+34T>G
NM_001136113.2:c.1825+34T>G NP_001129585.1:n.1825+34T>G
NM_001136114.2:c.1474+34T>G NP_001129586.1:n.1474+34T>G
NM_001353193.2:c.1891+34T>G NP_001340122.2:n.1891+34T>G
NM_001353194.2:c.1663+34T>G NP_001340123.1:n.1663+34T>G
NM_001353195.2:c.1474+34T>G NP_001340124.1:n.1474+34T>G
NM_001353196.2:c.1735+34T>G NP_001340125.1:n.1735+34T>G
NM_001353197.2:c.1729+34T>G NP_001340126.2:n.1729+34T>G
NM_001353198.2:c.1729+34T>G NP_001340127.2:n.1729+34T>G
NM_001353199.2:c.1540+34T>G NP_001340128.2:n.1540+34T>G
NM_001353200.2:c.1369+34T>G NP_001340129.1:n.1369+34T>G
NM_001374689.1:c.1813+34T>G NP_001361618.1:n.1813+34T>G
NM_001374690.1:c.1606+34T>G NP_001361619.1:n.1606+34T>G
NM_001374691.1:c.1474+34T>G NP_001361620.1:n.1474+34T>G
NM_001374692.1:c.1474+34T>G NP_001361621.1:n.1474+34T>G
NM_001374693.1:c.1474+34T>G NP_001361622.1:n.1474+34T>G
NM_001374695.1:c.1435+34T>G NP_001361624.1:n.1435+34T>G
NM_007171.4:c.1891+34T>G NP_009102.4:n.1891+34T>G
NR_148391.2:n.1859+34T>G
NR_148392.2:n.2077+34T>G
NR_148393.2:n.1998+34T>G
NR_148394.2:n.1752+34T>G
NR_148395.2:n.2150+34T>G
NR_148396.2:n.1784+34T>G
NR_148397.2:n.1909+34T>G
NR_148398.2:n.1864+34T>G
NR_148399.2:n.2390+34T>G
NR_148400.2:n.1989+34T>G