Canonical Allele Identifier: CA375315134
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522995C>G , CM000671.2:g.131522995C>G GRCh38
NC_000009.11:g.134398382C>G , CM000671.1:g.134398382C>G GRCh37
NC_000009.10:g.133388203C>G NCBI36
NG_008896.1:g.25094C>G
NG_008896.2:g.25094C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1905C>G ENSP00000343034.7:p.His635Gln
ENST00000404875.7:n.2607C>G
ENST00000423007.6:c.2124C>G ENSP00000404119.2:p.His708Gln
ENST00000677295.2:c.*2411C>G ENSP00000504346.2:n.*2411C>G
ENST00000678264.2:c.*2250C>G ENSP00000503157.2:n.*2250C>G
ENST00000682070.1:n.2377C>G
ENST00000682639.1:c.64C>G
ENST00000682813.1:n.2464C>G
ENST00000683231.1:c.64C>G
ENST00000683392.1:n.4659C>G
ENST00000683712.1:n.2472C>G
ENST00000683900.1:n.3967C>G
ENST00000684062.1:n.2733C>G
ENST00000684399.1:c.64C>G
ENST00000684579.1:n.3913C>G
ENST00000341012.12:c.1905C>G ENSP00000343034.7:p.His635Gln
ENST00000372220.5:c.936C>G ENSP00000361294.5:p.His312Gln
ENST00000372228.9:c.2133C>G ENSP00000361302.3:p.His711Gln
ENST00000402686.8:c.2067C>G MANE Select ENSP00000385797.4:p.His689Gln
ENST00000676640.1:c.2067C>G ENSP00000503281.1:p.His689Gln
ENST00000676803.1:c.1128C>G ENSP00000503093.1:p.His376Gln
ENST00000676835.1:c.*1282C>G ENSP00000502911.1:n.*1282C>G
ENST00000677029.1:c.1611C>G ENSP00000502936.1:p.His537Gln
ENST00000677099.1:c.*1777C>G ENSP00000504553.1:n.*1777C>G
ENST00000677216.1:c.1716C>G ENSP00000503772.1:p.His572Gln
ENST00000677221.1:n.1092C>G
ENST00000677295.1:c.*1289C>G ENSP00000504346.1:n.*1289C>G
ENST00000677444.1:c.2012C>G
ENST00000677586.1:n.1434C>G
ENST00000677626.1:c.1716C>G ENSP00000503552.1:p.His572Gln
ENST00000677853.1:c.*1075C>G ENSP00000503488.1:n.*1075C>G
ENST00000678264.1:c.*1444C>G ENSP00000503157.1:n.*1444C>G
ENST00000678303.1:c.1977C>G ENSP00000503696.1:p.His659Gln
ENST00000678366.1:c.*2316C>G ENSP00000504353.1:n.*2316C>G
ENST00000678546.1:c.*2012C>G ENSP00000503062.1:n.*2012C>G
ENST00000678548.1:c.*2206C>G ENSP00000503934.1:n.*2206C>G
ENST00000678626.1:n.1903C>G
ENST00000678739.1:c.*2233C>G ENSP00000503806.1:n.*2233C>G
ENST00000678833.1:c.*1819C>G ENSP00000503893.1:n.*1819C>G
ENST00000679023.1:c.1905C>G ENSP00000503718.1:p.His635Gln
ENST00000679076.1:c.1686C>G
ENST00000679111.1:c.*823C>G ENSP00000504257.1:n.*823C>G
ENST00000679189.1:c.1716C>G ENSP00000503356.1:p.His572Gln
ENST00000341012.11:c.1905C>G ENSP00000343034.7:p.His635Gln
ENST00000372220.4:c.930C>G ENSP00000361294.4:p.His310Gln
ENST00000372228.7:c.2133C>G ENSP00000361302.3:p.His711Gln
ENST00000402686.7:c.2067C>G ENSP00000385797.3:p.His689Gln
ENST00000404875.6:c.1716C>G ENSP00000384531.2:p.His572Gln
ENST00000423007.5:c.2067C>G ENSP00000404119.1:p.His689Gln
ENST00000485278.5:n.2617C>G
NM_001077365.1:c.2067C>G NP_001070833.1:p.His689Gln
NM_001077366.1:c.1905C>G NP_001070834.1:p.His635Gln
NM_001136113.1:c.2067C>G NP_001129585.1:p.His689Gln
NM_001136114.1:c.1716C>G NP_001129586.1:p.His572Gln
NM_007171.3:c.2133C>G NP_009102.3:p.His711Gln
XM_005272156.1:c.2133C>G XP_005272213.1:p.His711Gln
XM_005272158.1:c.1971C>G XP_005272215.1:p.His657Gln
XM_005272159.1:c.1782C>G XP_005272216.1:p.His594Gln
XM_005272162.1:c.936C>G XP_005272219.1:p.His312Gln
XM_006716932.1:c.1782C>G XP_006716995.1:p.His594Gln
XM_011518140.1:c.1986C>G XP_011516442.1:p.His662Gln
XM_011518141.1:c.1920C>G XP_011516443.1:p.His640Gln
XM_011518142.1:c.1824C>G XP_011516444.1:p.His608Gln
XM_011518143.1:c.1818C>G XP_011516445.1:p.His606Gln
XM_011518145.1:c.1677C>G XP_011516447.1:p.His559Gln
XM_011518147.1:c.1005C>G XP_011516449.1:p.His335Gln
XR_929703.1:n.2309C>G
NM_001353193.1:c.2133C>G NP_001340122.1:p.His711Gln
NM_001353194.1:c.1905C>G NP_001340123.1:p.His635Gln
NM_001353195.1:c.1716C>G NP_001340124.1:p.His572Gln
NM_001353196.1:c.1977C>G NP_001340125.1:p.His659Gln
NM_001353197.1:c.1971C>G NP_001340126.1:p.His657Gln
NM_001353198.1:c.1971C>G NP_001340127.1:p.His657Gln
NM_001353199.1:c.1782C>G NP_001340128.1:p.His594Gln
NM_001353200.1:c.1611C>G NP_001340129.1:p.His537Gln
NR_148391.1:n.2117C>G
NR_148392.1:n.2335C>G
NR_148393.1:n.2256C>G
NR_148394.1:n.2010C>G
NR_148395.1:n.2408C>G
NR_148396.1:n.2042C>G
NR_148397.1:n.2167C>G
NR_148398.1:n.2122C>G
NR_148399.1:n.2648C>G
NR_148400.1:n.2247C>G
XM_005272162.3:c.936C>G XP_005272219.1:p.His312Gln
XM_006716932.2:c.1782C>G XP_006716995.1:p.His594Gln
XM_011518140.2:c.1986C>G XP_011516442.1:p.His662Gln
XM_011518141.2:c.1920C>G XP_011516443.1:p.His640Gln
XM_011518142.2:c.1824C>G XP_011516444.1:p.His608Gln
XM_011518143.2:c.1818C>G XP_011516445.1:p.His606Gln
XM_011518145.2:c.1677C>G XP_011516447.1:p.His559Gln
XM_017014205.2:c.936C>G XP_016869694.1:p.His312Gln
XM_024447380.1:c.936C>G XP_024303148.1:p.His312Gln
XM_024447381.1:c.1242C>G XP_024303149.1:p.His414Gln
XM_024447382.1:c.936C>G XP_024303150.1:p.His312Gln
XR_001746160.2:n.2237C>G
XR_001746162.2:n.2442C>G
XR_001746164.1:n.2159C>G
XR_001746166.2:n.2454C>G
NM_001077365.2:c.2067C>G MANE Select NP_001070833.1:p.His689Gln
NM_001077366.2:c.1905C>G NP_001070834.1:p.His635Gln
NM_001136113.2:c.2067C>G NP_001129585.1:p.His689Gln
NM_001136114.2:c.1716C>G NP_001129586.1:p.His572Gln
NM_001353193.2:c.2133C>G NP_001340122.2:p.His711Gln
NM_001353194.2:c.1905C>G NP_001340123.1:p.His635Gln
NM_001353195.2:c.1716C>G NP_001340124.1:p.His572Gln
NM_001353196.2:c.1977C>G NP_001340125.1:p.His659Gln
NM_001353197.2:c.1971C>G NP_001340126.2:p.His657Gln
NM_001353198.2:c.1971C>G NP_001340127.2:p.His657Gln
NM_001353199.2:c.1782C>G NP_001340128.2:p.His594Gln
NM_001353200.2:c.1611C>G NP_001340129.1:p.His537Gln
NM_001374689.1:c.2055C>G NP_001361618.1:p.His685Gln
NM_001374690.1:c.1848C>G NP_001361619.1:p.His616Gln
NM_001374691.1:c.1716C>G NP_001361620.1:p.His572Gln
NM_001374692.1:c.1716C>G NP_001361621.1:p.His572Gln
NM_001374693.1:c.1716C>G NP_001361622.1:p.His572Gln
NM_001374695.1:c.1677C>G NP_001361624.1:p.His559Gln
NM_007171.4:c.2133C>G NP_009102.4:p.His711Gln
NR_148391.2:n.2101C>G
NR_148392.2:n.2319C>G
NR_148393.2:n.2240C>G
NR_148394.2:n.1994C>G
NR_148395.2:n.2392C>G
NR_148396.2:n.2026C>G
NR_148397.2:n.2151C>G
NR_148398.2:n.2106C>G
NR_148399.2:n.2632C>G
NR_148400.2:n.2231C>G