Canonical Allele Identifier: CA375315357
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523060C>A , CM000671.2:g.131523060C>A GRCh38
NC_000009.11:g.134398447C>A , CM000671.1:g.134398447C>A GRCh37
NC_000009.10:g.133388268C>A NCBI36
NG_008896.1:g.25159C>A
NG_008896.2:g.25159C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1970C>A ENSP00000343034.7:p.Ala657Asp
ENST00000404875.7:n.2672C>A
ENST00000423007.6:c.2189C>A ENSP00000404119.2:p.Ala730Asp
ENST00000677295.2:c.*2476C>A ENSP00000504346.2:n.*2476C>A
ENST00000678264.2:c.*2315C>A ENSP00000503157.2:n.*2315C>A
ENST00000682070.1:n.2442C>A
ENST00000682639.1:c.129C>A
ENST00000682813.1:n.2529C>A
ENST00000683231.1:c.129C>A
ENST00000683392.1:n.4724C>A
ENST00000683712.1:n.2537C>A
ENST00000683900.1:n.4032C>A
ENST00000684062.1:n.2798C>A
ENST00000684399.1:c.129C>A
ENST00000684579.1:n.3978C>A
ENST00000341012.12:c.1970C>A ENSP00000343034.7:p.Ala657Asp
ENST00000372220.5:c.1001C>A ENSP00000361294.5:p.Ala334Asp
ENST00000372228.9:c.2198C>A ENSP00000361302.3:p.Ala733Asp
ENST00000402686.8:c.2132C>A MANE Select ENSP00000385797.4:p.Ala711Asp
ENST00000676640.1:c.2132C>A ENSP00000503281.1:p.Ala711Asp
ENST00000676803.1:c.1193C>A ENSP00000503093.1:p.Ala398Asp
ENST00000676835.1:c.*1347C>A ENSP00000502911.1:n.*1347C>A
ENST00000677029.1:c.1676C>A ENSP00000502936.1:p.Ala559Asp
ENST00000677099.1:c.*1842C>A ENSP00000504553.1:n.*1842C>A
ENST00000677216.1:c.1781C>A ENSP00000503772.1:p.Ala594Asp
ENST00000677295.1:c.*1354C>A ENSP00000504346.1:n.*1354C>A
ENST00000677444.1:c.2077C>A
ENST00000677586.1:n.1499C>A
ENST00000677626.1:c.1781C>A ENSP00000503552.1:p.Ala594Asp
ENST00000677853.1:c.*1140C>A ENSP00000503488.1:n.*1140C>A
ENST00000678264.1:c.*1509C>A ENSP00000503157.1:n.*1509C>A
ENST00000678303.1:c.2042C>A ENSP00000503696.1:p.Ala681Asp
ENST00000678366.1:c.*2381C>A ENSP00000504353.1:n.*2381C>A
ENST00000678546.1:c.*2077C>A ENSP00000503062.1:n.*2077C>A
ENST00000678548.1:c.*2271C>A ENSP00000503934.1:n.*2271C>A
ENST00000678626.1:n.1968C>A
ENST00000678739.1:c.*2298C>A ENSP00000503806.1:n.*2298C>A
ENST00000678833.1:c.*1884C>A ENSP00000503893.1:n.*1884C>A
ENST00000679023.1:c.1970C>A ENSP00000503718.1:p.Ala657Asp
ENST00000679076.1:c.1751C>A
ENST00000679111.1:c.*888C>A ENSP00000504257.1:n.*888C>A
ENST00000679189.1:c.1781C>A ENSP00000503356.1:p.Ala594Asp
ENST00000341012.11:c.1970C>A ENSP00000343034.7:p.Ala657Asp
ENST00000372220.4:c.995C>A ENSP00000361294.4:p.Ala332Asp
ENST00000372228.7:c.2198C>A ENSP00000361302.3:p.Ala733Asp
ENST00000402686.7:c.2132C>A ENSP00000385797.3:p.Ala711Asp
ENST00000404875.6:c.1781C>A ENSP00000384531.2:p.Ala594Asp
ENST00000423007.5:c.2132C>A ENSP00000404119.1:p.Ala711Asp
ENST00000485278.5:n.2682C>A
NM_001077365.1:c.2132C>A NP_001070833.1:p.Ala711Asp
NM_001077366.1:c.1970C>A NP_001070834.1:p.Ala657Asp
NM_001136113.1:c.2132C>A NP_001129585.1:p.Ala711Asp
NM_001136114.1:c.1781C>A NP_001129586.1:p.Ala594Asp
NM_007171.3:c.2198C>A NP_009102.3:p.Ala733Asp
XM_005272156.1:c.2198C>A XP_005272213.1:p.Ala733Asp
XM_005272158.1:c.2036C>A XP_005272215.1:p.Ala679Asp
XM_005272159.1:c.1847C>A XP_005272216.1:p.Ala616Asp
XM_005272162.1:c.1001C>A XP_005272219.1:p.Ala334Asp
XM_006716932.1:c.1847C>A XP_006716995.1:p.Ala616Asp
XM_011518140.1:c.2051C>A XP_011516442.1:p.Ala684Asp
XM_011518141.1:c.1985C>A XP_011516443.1:p.Ala662Asp
XM_011518142.1:c.1889C>A XP_011516444.1:p.Ala630Asp
XM_011518143.1:c.1883C>A XP_011516445.1:p.Ala628Asp
XM_011518145.1:c.1742C>A XP_011516447.1:p.Ala581Asp
XM_011518147.1:c.1070C>A XP_011516449.1:p.Ala357Asp
XR_929703.1:n.2374C>A
NM_001353193.1:c.2198C>A NP_001340122.1:p.Ala733Asp
NM_001353194.1:c.1970C>A NP_001340123.1:p.Ala657Asp
NM_001353195.1:c.1781C>A NP_001340124.1:p.Ala594Asp
NM_001353196.1:c.2042C>A NP_001340125.1:p.Ala681Asp
NM_001353197.1:c.2036C>A NP_001340126.1:p.Ala679Asp
NM_001353198.1:c.2036C>A NP_001340127.1:p.Ala679Asp
NM_001353199.1:c.1847C>A NP_001340128.1:p.Ala616Asp
NM_001353200.1:c.1676C>A NP_001340129.1:p.Ala559Asp
NR_148391.1:n.2182C>A
NR_148392.1:n.2400C>A
NR_148393.1:n.2321C>A
NR_148394.1:n.2075C>A
NR_148395.1:n.2473C>A
NR_148396.1:n.2107C>A
NR_148397.1:n.2232C>A
NR_148398.1:n.2187C>A
NR_148399.1:n.2713C>A
NR_148400.1:n.2312C>A
XM_005272162.3:c.1001C>A XP_005272219.1:p.Ala334Asp
XM_006716932.2:c.1847C>A XP_006716995.1:p.Ala616Asp
XM_011518140.2:c.2051C>A XP_011516442.1:p.Ala684Asp
XM_011518141.2:c.1985C>A XP_011516443.1:p.Ala662Asp
XM_011518142.2:c.1889C>A XP_011516444.1:p.Ala630Asp
XM_011518143.2:c.1883C>A XP_011516445.1:p.Ala628Asp
XM_011518145.2:c.1742C>A XP_011516447.1:p.Ala581Asp
XM_017014205.2:c.1001C>A XP_016869694.1:p.Ala334Asp
XM_024447380.1:c.1001C>A XP_024303148.1:p.Ala334Asp
XM_024447381.1:c.1307C>A XP_024303149.1:p.Ala436Asp
XM_024447382.1:c.1001C>A XP_024303150.1:p.Ala334Asp
XR_001746160.2:n.2302C>A
XR_001746162.2:n.2507C>A
XR_001746164.1:n.2224C>A
XR_001746166.2:n.2519C>A
NM_001077365.2:c.2132C>A MANE Select NP_001070833.1:p.Ala711Asp
NM_001077366.2:c.1970C>A NP_001070834.1:p.Ala657Asp
NM_001136113.2:c.2132C>A NP_001129585.1:p.Ala711Asp
NM_001136114.2:c.1781C>A NP_001129586.1:p.Ala594Asp
NM_001353193.2:c.2198C>A NP_001340122.2:p.Ala733Asp
NM_001353194.2:c.1970C>A NP_001340123.1:p.Ala657Asp
NM_001353195.2:c.1781C>A NP_001340124.1:p.Ala594Asp
NM_001353196.2:c.2042C>A NP_001340125.1:p.Ala681Asp
NM_001353197.2:c.2036C>A NP_001340126.2:p.Ala679Asp
NM_001353198.2:c.2036C>A NP_001340127.2:p.Ala679Asp
NM_001353199.2:c.1847C>A NP_001340128.2:p.Ala616Asp
NM_001353200.2:c.1676C>A NP_001340129.1:p.Ala559Asp
NM_001374689.1:c.2120C>A NP_001361618.1:p.Ala707Asp
NM_001374690.1:c.1913C>A NP_001361619.1:p.Ala638Asp
NM_001374691.1:c.1781C>A NP_001361620.1:p.Ala594Asp
NM_001374692.1:c.1781C>A NP_001361621.1:p.Ala594Asp
NM_001374693.1:c.1781C>A NP_001361622.1:p.Ala594Asp
NM_001374695.1:c.1742C>A NP_001361624.1:p.Ala581Asp
NM_007171.4:c.2198C>A NP_009102.4:p.Ala733Asp
NR_148391.2:n.2166C>A
NR_148392.2:n.2384C>A
NR_148393.2:n.2305C>A
NR_148394.2:n.2059C>A
NR_148395.2:n.2457C>A
NR_148396.2:n.2091C>A
NR_148397.2:n.2216C>A
NR_148398.2:n.2171C>A
NR_148399.2:n.2697C>A
NR_148400.2:n.2296C>A