Canonical Allele Identifier: CA375314621
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522185T>G , CM000671.2:g.131522185T>G GRCh38
NC_000009.11:g.134397572T>G , CM000671.1:g.134397572T>G GRCh37
NC_000009.10:g.133387393T>G NCBI36
NG_008896.1:g.24284T>G
NG_008896.2:g.24284T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1802T>G ENSP00000343034.7:p.Leu601Arg
ENST00000404875.7:n.2504T>G
ENST00000423007.6:c.2021T>G ENSP00000404119.2:p.Leu674Arg
ENST00000677295.2:c.*2308T>G ENSP00000504346.2:n.*2308T>G
ENST00000678264.2:c.*2147T>G ENSP00000503157.2:n.*2147T>G
ENST00000682070.1:n.2291-17T>G
ENST00000682813.1:n.2368T>G
ENST00000683392.1:n.4573-17T>G
ENST00000683712.1:n.2369T>G
ENST00000683900.1:n.3864T>G
ENST00000684062.1:n.2630T>G
ENST00000684579.1:n.3810T>G
ENST00000684679.1:n.1191T>G
ENST00000341012.12:c.1802T>G ENSP00000343034.7:p.Leu601Arg
ENST00000372220.5:c.833T>G ENSP00000361294.5:p.Leu278Arg
ENST00000372228.9:c.2030T>G ENSP00000361302.3:p.Leu677Arg
ENST00000402686.8:c.1964T>G MANE Select ENSP00000385797.4:p.Leu655Arg
ENST00000676640.1:c.1964T>G ENSP00000503281.1:p.Leu655Arg
ENST00000676803.1:c.1025T>G ENSP00000503093.1:p.Leu342Arg
ENST00000676835.1:c.*1179T>G ENSP00000502911.1:n.*1179T>G
ENST00000677029.1:c.1508T>G ENSP00000502936.1:p.Leu503Arg
ENST00000677099.1:c.*1674T>G ENSP00000504553.1:n.*1674T>G
ENST00000677216.1:c.1613T>G ENSP00000503772.1:p.Leu538Arg
ENST00000677221.1:n.989T>G
ENST00000677295.1:c.*1203-17T>G ENSP00000504346.1:n.*1203-17T>G
ENST00000677444.1:c.1909T>G
ENST00000677586.1:n.1331T>G
ENST00000677626.1:c.1613T>G ENSP00000503552.1:p.Leu538Arg
ENST00000677853.1:c.*972T>G ENSP00000503488.1:n.*972T>G
ENST00000678202.1:n.1123T>G
ENST00000678264.1:c.*1341T>G ENSP00000503157.1:n.*1341T>G
ENST00000678303.1:c.1874T>G ENSP00000503696.1:p.Leu625Arg
ENST00000678366.1:c.*2213T>G ENSP00000504353.1:n.*2213T>G
ENST00000678546.1:c.*1909T>G ENSP00000503062.1:n.*1909T>G
ENST00000678548.1:c.*2103T>G ENSP00000503934.1:n.*2103T>G
ENST00000678626.1:n.1800T>G
ENST00000678739.1:c.*2147-17T>G ENSP00000503806.1:n.*2147-17T>G
ENST00000678833.1:c.*1716T>G ENSP00000503893.1:n.*1716T>G
ENST00000679023.1:c.1802T>G ENSP00000503718.1:p.Leu601Arg
ENST00000679076.1:c.1583T>G
ENST00000679111.1:c.*720T>G ENSP00000504257.1:n.*720T>G
ENST00000679189.1:c.1613T>G ENSP00000503356.1:p.Leu538Arg
ENST00000341012.11:c.1802T>G ENSP00000343034.7:p.Leu601Arg
ENST00000372220.4:c.827T>G ENSP00000361294.4:p.Leu276Arg
ENST00000372228.7:c.2030T>G ENSP00000361302.3:p.Leu677Arg
ENST00000402686.7:c.1964T>G ENSP00000385797.3:p.Leu655Arg
ENST00000404875.6:c.1613T>G ENSP00000384531.2:p.Leu538Arg
ENST00000423007.5:c.1964T>G ENSP00000404119.1:p.Leu655Arg
ENST00000485278.5:n.2514T>G
ENST00000494883.1:n.507T>G
NM_001077365.1:c.1964T>G NP_001070833.1:p.Leu655Arg
NM_001077366.1:c.1802T>G NP_001070834.1:p.Leu601Arg
NM_001136113.1:c.1964T>G NP_001129585.1:p.Leu655Arg
NM_001136114.1:c.1613T>G NP_001129586.1:p.Leu538Arg
NM_007171.3:c.2030T>G NP_009102.3:p.Leu677Arg
XM_005272156.1:c.2030T>G XP_005272213.1:p.Leu677Arg
XM_005272158.1:c.1868T>G XP_005272215.1:p.Leu623Arg
XM_005272159.1:c.1679T>G XP_005272216.1:p.Leu560Arg
XM_005272162.1:c.833T>G XP_005272219.1:p.Leu278Arg
XM_006716932.1:c.1679T>G XP_006716995.1:p.Leu560Arg
XM_011518140.1:c.1883T>G XP_011516442.1:p.Leu628Arg
XM_011518141.1:c.1817T>G XP_011516443.1:p.Leu606Arg
XM_011518142.1:c.1721T>G XP_011516444.1:p.Leu574Arg
XM_011518143.1:c.1715T>G XP_011516445.1:p.Leu572Arg
XM_011518145.1:c.1574T>G XP_011516447.1:p.Leu525Arg
XM_011518147.1:c.902T>G XP_011516449.1:p.Leu301Arg
XR_929703.1:n.2206T>G
NM_001353193.1:c.2030T>G NP_001340122.1:p.Leu677Arg
NM_001353194.1:c.1802T>G NP_001340123.1:p.Leu601Arg
NM_001353195.1:c.1613T>G NP_001340124.1:p.Leu538Arg
NM_001353196.1:c.1874T>G NP_001340125.1:p.Leu625Arg
NM_001353197.1:c.1868T>G NP_001340126.1:p.Leu623Arg
NM_001353198.1:c.1868T>G NP_001340127.1:p.Leu623Arg
NM_001353199.1:c.1679T>G NP_001340128.1:p.Leu560Arg
NM_001353200.1:c.1508T>G NP_001340129.1:p.Leu503Arg
NR_148391.1:n.2014T>G
NR_148392.1:n.2232T>G
NR_148393.1:n.2153T>G
NR_148394.1:n.1907T>G
NR_148395.1:n.2305T>G
NR_148396.1:n.1939T>G
NR_148397.1:n.2064T>G
NR_148398.1:n.2019T>G
NR_148399.1:n.2545T>G
NR_148400.1:n.2144T>G
XM_005272162.3:c.833T>G XP_005272219.1:p.Leu278Arg
XM_006716932.2:c.1679T>G XP_006716995.1:p.Leu560Arg
XM_011518140.2:c.1883T>G XP_011516442.1:p.Leu628Arg
XM_011518141.2:c.1817T>G XP_011516443.1:p.Leu606Arg
XM_011518142.2:c.1721T>G XP_011516444.1:p.Leu574Arg
XM_011518143.2:c.1715T>G XP_011516445.1:p.Leu572Arg
XM_011518145.2:c.1574T>G XP_011516447.1:p.Leu525Arg
XM_017014205.2:c.833T>G XP_016869694.1:p.Leu278Arg
XM_024447380.1:c.833T>G XP_024303148.1:p.Leu278Arg
XM_024447381.1:c.1139T>G XP_024303149.1:p.Leu380Arg
XM_024447382.1:c.833T>G XP_024303150.1:p.Leu278Arg
XR_001746160.2:n.2134T>G
XR_001746162.2:n.2339T>G
XR_001746164.1:n.2056T>G
XR_001746166.2:n.2351T>G
NM_001077365.2:c.1964T>G MANE Select NP_001070833.1:p.Leu655Arg
NM_001077366.2:c.1802T>G NP_001070834.1:p.Leu601Arg
NM_001136113.2:c.1964T>G NP_001129585.1:p.Leu655Arg
NM_001136114.2:c.1613T>G NP_001129586.1:p.Leu538Arg
NM_001353193.2:c.2030T>G NP_001340122.2:p.Leu677Arg
NM_001353194.2:c.1802T>G NP_001340123.1:p.Leu601Arg
NM_001353195.2:c.1613T>G NP_001340124.1:p.Leu538Arg
NM_001353196.2:c.1874T>G NP_001340125.1:p.Leu625Arg
NM_001353197.2:c.1868T>G NP_001340126.2:p.Leu623Arg
NM_001353198.2:c.1868T>G NP_001340127.2:p.Leu623Arg
NM_001353199.2:c.1679T>G NP_001340128.2:p.Leu560Arg
NM_001353200.2:c.1508T>G NP_001340129.1:p.Leu503Arg
NM_001374689.1:c.1952T>G NP_001361618.1:p.Leu651Arg
NM_001374690.1:c.1745T>G NP_001361619.1:p.Leu582Arg
NM_001374691.1:c.1613T>G NP_001361620.1:p.Leu538Arg
NM_001374692.1:c.1613T>G NP_001361621.1:p.Leu538Arg
NM_001374693.1:c.1613T>G NP_001361622.1:p.Leu538Arg
NM_001374695.1:c.1574T>G NP_001361624.1:p.Leu525Arg
NM_007171.4:c.2030T>G NP_009102.4:p.Leu677Arg
NR_148391.2:n.1998T>G
NR_148392.2:n.2216T>G
NR_148393.2:n.2137T>G
NR_148394.2:n.1891T>G
NR_148395.2:n.2289T>G
NR_148396.2:n.1923T>G
NR_148397.2:n.2048T>G
NR_148398.2:n.2003T>G
NR_148399.2:n.2529T>G
NR_148400.2:n.2128T>G