Canonical Allele Identifier: CA375312092
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518937A>T , CM000671.2:g.131518937A>T GRCh38
NC_000009.11:g.134394324A>T , CM000671.1:g.134394324A>T GRCh37
NC_000009.10:g.133384145A>T NCBI36
NG_008896.1:g.21036A>T
NG_008896.2:g.21036A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1304A>T ENSP00000343034.7:p.Glu435Val
ENST00000404875.7:n.2006A>T
ENST00000423007.6:c.1523A>T ENSP00000404119.2:p.Glu508Val
ENST00000677295.2:c.*1810A>T ENSP00000504346.2:n.*1810A>T
ENST00000678264.2:c.*1649A>T ENSP00000503157.2:n.*1649A>T
ENST00000682070.1:n.1931A>T
ENST00000682539.1:c.404A>T
ENST00000682813.1:n.1870A>T
ENST00000683392.1:n.4213A>T
ENST00000683712.1:n.1871A>T
ENST00000683900.1:n.3366A>T
ENST00000684062.1:n.2132A>T
ENST00000684579.1:n.3312A>T
ENST00000684679.1:n.693A>T
ENST00000341012.12:c.1304A>T ENSP00000343034.7:p.Glu435Val
ENST00000372220.5:c.335A>T ENSP00000361294.5:p.Glu112Val
ENST00000372228.9:c.1532A>T ENSP00000361302.3:p.Glu511Val
ENST00000402686.8:c.1466A>T MANE Select ENSP00000385797.4:p.Glu489Val
ENST00000676640.1:c.1466A>T ENSP00000503281.1:p.Glu489Val
ENST00000676803.1:c.641A>T ENSP00000503093.1:p.Glu214Val
ENST00000676835.1:c.*681A>T ENSP00000502911.1:n.*681A>T
ENST00000677029.1:c.1010A>T ENSP00000502936.1:p.Glu337Val
ENST00000677099.1:c.*1176A>T ENSP00000504553.1:n.*1176A>T
ENST00000677216.1:c.1115A>T ENSP00000503772.1:p.Glu372Val
ENST00000677221.1:n.491A>T
ENST00000677295.1:c.*843A>T ENSP00000504346.1:n.*843A>T
ENST00000677444.1:c.1411A>T
ENST00000677586.1:n.947A>T
ENST00000677626.1:c.1115A>T ENSP00000503552.1:p.Glu372Val
ENST00000677677.1:n.1426A>T
ENST00000677853.1:c.*474A>T ENSP00000503488.1:n.*474A>T
ENST00000678202.1:n.625A>T
ENST00000678264.1:c.*843A>T ENSP00000503157.1:n.*843A>T
ENST00000678303.1:c.1376A>T ENSP00000503696.1:p.Glu459Val
ENST00000678366.1:c.*1715A>T ENSP00000504353.1:n.*1715A>T
ENST00000678546.1:c.*1411A>T ENSP00000503062.1:n.*1411A>T
ENST00000678548.1:c.*1538A>T ENSP00000503934.1:n.*1538A>T
ENST00000678626.1:n.1302A>T
ENST00000678733.1:c.547A>T
ENST00000678739.1:c.*1792A>T ENSP00000503806.1:n.*1792A>T
ENST00000678833.1:c.*913A>T ENSP00000503893.1:n.*913A>T
ENST00000679023.1:c.1304A>T ENSP00000503718.1:p.Glu435Val
ENST00000679076.1:c.1085A>T
ENST00000679111.1:c.*222A>T ENSP00000504257.1:n.*222A>T
ENST00000679189.1:c.1115A>T ENSP00000503356.1:p.Glu372Val
ENST00000341012.11:c.1304A>T ENSP00000343034.7:p.Glu435Val
ENST00000372220.4:c.329A>T ENSP00000361294.4:p.Glu110Val
ENST00000372228.7:c.1532A>T ENSP00000361302.3:p.Glu511Val
ENST00000402686.7:c.1466A>T ENSP00000385797.3:p.Glu489Val
ENST00000404875.6:c.1115A>T ENSP00000384531.2:p.Glu372Val
ENST00000423007.5:c.1466A>T ENSP00000404119.1:p.Glu489Val
ENST00000467848.1:n.170A>T
ENST00000485278.5:n.2021A>T
NM_001077365.1:c.1466A>T NP_001070833.1:p.Glu489Val
NM_001077366.1:c.1304A>T NP_001070834.1:p.Glu435Val
NM_001136113.1:c.1466A>T NP_001129585.1:p.Glu489Val
NM_001136114.1:c.1115A>T NP_001129586.1:p.Glu372Val
NM_007171.3:c.1532A>T NP_009102.3:p.Glu511Val
XM_005272156.1:c.1532A>T XP_005272213.1:p.Glu511Val
XM_005272158.1:c.1370A>T XP_005272215.1:p.Glu457Val
XM_005272159.1:c.1181A>T XP_005272216.1:p.Glu394Val
XM_005272162.1:c.335A>T XP_005272219.1:p.Glu112Val
XM_006716932.1:c.1181A>T XP_006716995.1:p.Glu394Val
XM_011518140.1:c.1385A>T XP_011516442.1:p.Glu462Val
XM_011518141.1:c.1319A>T XP_011516443.1:p.Glu440Val
XM_011518142.1:c.1223A>T XP_011516444.1:p.Glu408Val
XM_011518143.1:c.1217A>T XP_011516445.1:p.Glu406Val
XM_011518145.1:c.1076A>T XP_011516447.1:p.Glu359Val
XM_011518147.1:c.404A>T XP_011516449.1:p.Glu135Val
XR_929703.1:n.1708A>T
NM_001353193.1:c.1532A>T NP_001340122.1:p.Glu511Val
NM_001353194.1:c.1304A>T NP_001340123.1:p.Glu435Val
NM_001353195.1:c.1115A>T NP_001340124.1:p.Glu372Val
NM_001353196.1:c.1376A>T NP_001340125.1:p.Glu459Val
NM_001353197.1:c.1370A>T NP_001340126.1:p.Glu457Val
NM_001353198.1:c.1370A>T NP_001340127.1:p.Glu457Val
NM_001353199.1:c.1181A>T NP_001340128.1:p.Glu394Val
NM_001353200.1:c.1010A>T NP_001340129.1:p.Glu337Val
NR_148391.1:n.1516A>T
NR_148392.1:n.1734A>T
NR_148393.1:n.1655A>T
NR_148394.1:n.1409A>T
NR_148395.1:n.1807A>T
NR_148396.1:n.1441A>T
NR_148397.1:n.1566A>T
NR_148398.1:n.1521A>T
NR_148399.1:n.2047A>T
NR_148400.1:n.1646A>T
XM_005272162.3:c.335A>T XP_005272219.1:p.Glu112Val
XM_006716932.2:c.1181A>T XP_006716995.1:p.Glu394Val
XM_011518140.2:c.1385A>T XP_011516442.1:p.Glu462Val
XM_011518141.2:c.1319A>T XP_011516443.1:p.Glu440Val
XM_011518142.2:c.1223A>T XP_011516444.1:p.Glu408Val
XM_011518143.2:c.1217A>T XP_011516445.1:p.Glu406Val
XM_011518145.2:c.1076A>T XP_011516447.1:p.Glu359Val
XM_017014205.2:c.335A>T XP_016869694.1:p.Glu112Val
XM_024447380.1:c.335A>T XP_024303148.1:p.Glu112Val
XM_024447381.1:c.641A>T XP_024303149.1:p.Glu214Val
XM_024447382.1:c.335A>T XP_024303150.1:p.Glu112Val
XR_001746160.2:n.1636A>T
XR_001746162.2:n.1841A>T
XR_001746164.1:n.1558A>T
XR_001746166.2:n.1853A>T
NM_001077365.2:c.1466A>T MANE Select NP_001070833.1:p.Glu489Val
NM_001077366.2:c.1304A>T NP_001070834.1:p.Glu435Val
NM_001136113.2:c.1466A>T NP_001129585.1:p.Glu489Val
NM_001136114.2:c.1115A>T NP_001129586.1:p.Glu372Val
NM_001353193.2:c.1532A>T NP_001340122.2:p.Glu511Val
NM_001353194.2:c.1304A>T NP_001340123.1:p.Glu435Val
NM_001353195.2:c.1115A>T NP_001340124.1:p.Glu372Val
NM_001353196.2:c.1376A>T NP_001340125.1:p.Glu459Val
NM_001353197.2:c.1370A>T NP_001340126.2:p.Glu457Val
NM_001353198.2:c.1370A>T NP_001340127.2:p.Glu457Val
NM_001353199.2:c.1181A>T NP_001340128.2:p.Glu394Val
NM_001353200.2:c.1010A>T NP_001340129.1:p.Glu337Val
NM_001374689.1:c.1454A>T NP_001361618.1:p.Glu485Val
NM_001374690.1:c.1365+400A>T NP_001361619.1:n.1365+400A>T
NM_001374691.1:c.1115A>T NP_001361620.1:p.Glu372Val
NM_001374692.1:c.1115A>T NP_001361621.1:p.Glu372Val
NM_001374693.1:c.1115A>T NP_001361622.1:p.Glu372Val
NM_001374695.1:c.1076A>T NP_001361624.1:p.Glu359Val
NM_007171.4:c.1532A>T NP_009102.4:p.Glu511Val
NR_148391.2:n.1500A>T
NR_148392.2:n.1718A>T
NR_148393.2:n.1639A>T
NR_148394.2:n.1393A>T
NR_148395.2:n.1791A>T
NR_148396.2:n.1425A>T
NR_148397.2:n.1550A>T
NR_148398.2:n.1505A>T
NR_148399.2:n.2031A>T
NR_148400.2:n.1630A>T