Canonical Allele Identifier: CA1881752845
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518953C= , CM000671.2:g.131518953C= GRCh38
NC_000009.11:g.134394340C= , CM000671.1:g.134394340C= GRCh37
NC_000009.10:g.133384161C= NCBI36
NG_008896.1:g.21052C=
NG_008896.2:g.21052C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1320C= ENSP00000343034.7:p.Gly440=
ENST00000404875.7:n.2022C=
ENST00000423007.6:c.1539C= ENSP00000404119.2:p.Gly513=
ENST00000677295.2:c.*1826C= ENSP00000504346.2:n.*1826C=
ENST00000678264.2:c.*1665C= ENSP00000503157.2:n.*1665C=
ENST00000682070.1:n.1947C=
ENST00000682539.1:c.420C=
ENST00000682813.1:n.1886C=
ENST00000683392.1:n.4229C=
ENST00000683712.1:n.1887C=
ENST00000683900.1:n.3382C=
ENST00000684062.1:n.2148C=
ENST00000684579.1:n.3328C=
ENST00000684679.1:n.709C=
ENST00000341012.12:c.1320C= ENSP00000343034.7:p.Gly440=
ENST00000372220.5:c.351C= ENSP00000361294.5:p.Gly117=
ENST00000372228.9:c.1548C= ENSP00000361302.3:p.Gly516=
ENST00000402686.8:c.1482C= MANE Select ENSP00000385797.4:p.Gly494=
ENST00000676640.1:c.1482C= ENSP00000503281.1:p.Gly494=
ENST00000676803.1:c.657C= ENSP00000503093.1:p.Gly219=
ENST00000676835.1:c.*697C= ENSP00000502911.1:n.*697C=
ENST00000677029.1:c.1026C= ENSP00000502936.1:p.Gly342=
ENST00000677099.1:c.*1192C= ENSP00000504553.1:n.*1192C=
ENST00000677216.1:c.1131C= ENSP00000503772.1:p.Gly377=
ENST00000677221.1:n.507C=
ENST00000677295.1:c.*859C= ENSP00000504346.1:n.*859C=
ENST00000677444.1:c.1427C=
ENST00000677586.1:n.963C=
ENST00000677626.1:c.1131C= ENSP00000503552.1:p.Gly377=
ENST00000677677.1:n.1442C=
ENST00000677853.1:c.*490C= ENSP00000503488.1:n.*490C=
ENST00000678202.1:n.641C=
ENST00000678264.1:c.*859C= ENSP00000503157.1:n.*859C=
ENST00000678303.1:c.1392C= ENSP00000503696.1:p.Gly464=
ENST00000678366.1:c.*1731C= ENSP00000504353.1:n.*1731C=
ENST00000678546.1:c.*1427C= ENSP00000503062.1:n.*1427C=
ENST00000678548.1:c.*1554C= ENSP00000503934.1:n.*1554C=
ENST00000678626.1:n.1318C=
ENST00000678733.1:c.563C=
ENST00000678739.1:c.*1808C= ENSP00000503806.1:n.*1808C=
ENST00000678833.1:c.*929C= ENSP00000503893.1:n.*929C=
ENST00000679023.1:c.1320C= ENSP00000503718.1:p.Gly440=
ENST00000679076.1:c.1101C=
ENST00000679111.1:c.*238C= ENSP00000504257.1:n.*238C=
ENST00000679189.1:c.1131C= ENSP00000503356.1:p.Gly377=
ENST00000341012.11:c.1320C= ENSP00000343034.7:p.Gly440=
ENST00000372220.4:c.345C= ENSP00000361294.4:p.Gly115=
ENST00000372228.7:c.1548C= ENSP00000361302.3:p.Gly516=
ENST00000402686.7:c.1482C= ENSP00000385797.3:p.Gly494=
ENST00000404875.6:c.1131C= ENSP00000384531.2:p.Gly377=
ENST00000423007.5:c.1482C= ENSP00000404119.1:p.Gly494=
ENST00000467848.1:n.186C=
ENST00000485278.5:n.2037C=
NM_001077365.1:c.1482C= NP_001070833.1:p.Gly494=
NM_001077366.1:c.1320C= NP_001070834.1:p.Gly440=
NM_001136113.1:c.1482C= NP_001129585.1:p.Gly494=
NM_001136114.1:c.1131C= NP_001129586.1:p.Gly377=
NM_007171.3:c.1548C= NP_009102.3:p.Gly516=
XM_005272156.1:c.1548C= XP_005272213.1:p.Gly516=
XM_005272158.1:c.1386C= XP_005272215.1:p.Gly462=
XM_005272159.1:c.1197C= XP_005272216.1:p.Gly399=
XM_005272162.1:c.351C= XP_005272219.1:p.Gly117=
XM_006716932.1:c.1197C= XP_006716995.1:p.Gly399=
XM_011518140.1:c.1401C= XP_011516442.1:p.Gly467=
XM_011518141.1:c.1335C= XP_011516443.1:p.Gly445=
XM_011518142.1:c.1239C= XP_011516444.1:p.Gly413=
XM_011518143.1:c.1233C= XP_011516445.1:p.Gly411=
XM_011518145.1:c.1092C= XP_011516447.1:p.Gly364=
XM_011518147.1:c.420C= XP_011516449.1:p.Gly140=
XR_929703.1:n.1724C=
NM_001353193.1:c.1548C= NP_001340122.1:p.Gly516=
NM_001353194.1:c.1320C= NP_001340123.1:p.Gly440=
NM_001353195.1:c.1131C= NP_001340124.1:p.Gly377=
NM_001353196.1:c.1392C= NP_001340125.1:p.Gly464=
NM_001353197.1:c.1386C= NP_001340126.1:p.Gly462=
NM_001353198.1:c.1386C= NP_001340127.1:p.Gly462=
NM_001353199.1:c.1197C= NP_001340128.1:p.Gly399=
NM_001353200.1:c.1026C= NP_001340129.1:p.Gly342=
NR_148391.1:n.1532C=
NR_148392.1:n.1750C=
NR_148393.1:n.1671C=
NR_148394.1:n.1425C=
NR_148395.1:n.1823C=
NR_148396.1:n.1457C=
NR_148397.1:n.1582C=
NR_148398.1:n.1537C=
NR_148399.1:n.2063C=
NR_148400.1:n.1662C=
XM_005272162.3:c.351C= XP_005272219.1:p.Gly117=
XM_006716932.2:c.1197C= XP_006716995.1:p.Gly399=
XM_011518140.2:c.1401C= XP_011516442.1:p.Gly467=
XM_011518141.2:c.1335C= XP_011516443.1:p.Gly445=
XM_011518142.2:c.1239C= XP_011516444.1:p.Gly413=
XM_011518143.2:c.1233C= XP_011516445.1:p.Gly411=
XM_011518145.2:c.1092C= XP_011516447.1:p.Gly364=
XM_017014205.2:c.351C= XP_016869694.1:p.Gly117=
XM_024447380.1:c.351C= XP_024303148.1:p.Gly117=
XM_024447381.1:c.657C= XP_024303149.1:p.Gly219=
XM_024447382.1:c.351C= XP_024303150.1:p.Gly117=
XR_001746160.2:n.1652C=
XR_001746162.2:n.1857C=
XR_001746164.1:n.1574C=
XR_001746166.2:n.1869C=
NM_001077365.2:c.1482C= MANE Select NP_001070833.1:p.Gly494=
NM_001077366.2:c.1320C= NP_001070834.1:p.Gly440=
NM_001136113.2:c.1482C= NP_001129585.1:p.Gly494=
NM_001136114.2:c.1131C= NP_001129586.1:p.Gly377=
NM_001353193.2:c.1548C= NP_001340122.2:p.Gly516=
NM_001353194.2:c.1320C= NP_001340123.1:p.Gly440=
NM_001353195.2:c.1131C= NP_001340124.1:p.Gly377=
NM_001353196.2:c.1392C= NP_001340125.1:p.Gly464=
NM_001353197.2:c.1386C= NP_001340126.2:p.Gly462=
NM_001353198.2:c.1386C= NP_001340127.2:p.Gly462=
NM_001353199.2:c.1197C= NP_001340128.2:p.Gly399=
NM_001353200.2:c.1026C= NP_001340129.1:p.Gly342=
NM_001374689.1:c.1470C= NP_001361618.1:p.Gly490=
NM_001374690.1:c.1365+416C= NP_001361619.1:n.1365+416C=
NM_001374691.1:c.1131C= NP_001361620.1:p.Gly377=
NM_001374692.1:c.1131C= NP_001361621.1:p.Gly377=
NM_001374693.1:c.1131C= NP_001361622.1:p.Gly377=
NM_001374695.1:c.1092C= NP_001361624.1:p.Gly364=
NM_007171.4:c.1548C= NP_009102.4:p.Gly516=
NR_148391.2:n.1516C=
NR_148392.2:n.1734C=
NR_148393.2:n.1655C=
NR_148394.2:n.1409C=
NR_148395.2:n.1807C=
NR_148396.2:n.1441C=
NR_148397.2:n.1566C=
NR_148398.2:n.1521C=
NR_148399.2:n.2047C=
NR_148400.2:n.1646C=