Canonical Allele Identifier: CA375315426
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523078G>A , CM000671.2:g.131523078G>A GRCh38
NC_000009.11:g.134398465G>A , CM000671.1:g.134398465G>A GRCh37
NC_000009.10:g.133388286G>A NCBI36
NG_008896.1:g.25177G>A
NG_008896.2:g.25177G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1988G>A ENSP00000343034.7:p.Ser663Asn
ENST00000404875.7:n.2690G>A
ENST00000423007.6:c.2207G>A ENSP00000404119.2:p.Ser736Asn
ENST00000677295.2:c.*2494G>A ENSP00000504346.2:n.*2494G>A
ENST00000678264.2:c.*2333G>A ENSP00000503157.2:n.*2333G>A
ENST00000682070.1:n.2460G>A
ENST00000682639.1:c.147G>A
ENST00000682813.1:n.2547G>A
ENST00000683231.1:c.147G>A
ENST00000683392.1:n.4742G>A
ENST00000683712.1:n.2555G>A
ENST00000683900.1:n.4050G>A
ENST00000684062.1:n.2816G>A
ENST00000684399.1:c.147G>A
ENST00000684579.1:n.3996G>A
ENST00000341012.12:c.1988G>A ENSP00000343034.7:p.Ser663Asn
ENST00000372220.5:c.1019G>A ENSP00000361294.5:p.Ser340Asn
ENST00000372228.9:c.2216G>A ENSP00000361302.3:p.Ser739Asn
ENST00000402686.8:c.2150G>A MANE Select ENSP00000385797.4:p.Ser717Asn
ENST00000676640.1:c.2150G>A ENSP00000503281.1:p.Ser717Asn
ENST00000676803.1:c.1211G>A ENSP00000503093.1:p.Ser404Asn
ENST00000676835.1:c.*1365G>A ENSP00000502911.1:n.*1365G>A
ENST00000677029.1:c.1694G>A ENSP00000502936.1:p.Ser565Asn
ENST00000677099.1:c.*1860G>A ENSP00000504553.1:n.*1860G>A
ENST00000677216.1:c.1799G>A ENSP00000503772.1:p.Ser600Asn
ENST00000677295.1:c.*1372G>A ENSP00000504346.1:n.*1372G>A
ENST00000677444.1:c.2095G>A
ENST00000677586.1:n.1517G>A
ENST00000677626.1:c.1799G>A ENSP00000503552.1:p.Ser600Asn
ENST00000677853.1:c.*1158G>A ENSP00000503488.1:n.*1158G>A
ENST00000678264.1:c.*1527G>A ENSP00000503157.1:n.*1527G>A
ENST00000678303.1:c.2060G>A ENSP00000503696.1:p.Ser687Asn
ENST00000678366.1:c.*2399G>A ENSP00000504353.1:n.*2399G>A
ENST00000678546.1:c.*2095G>A ENSP00000503062.1:n.*2095G>A
ENST00000678548.1:c.*2289G>A ENSP00000503934.1:n.*2289G>A
ENST00000678626.1:n.1986G>A
ENST00000678739.1:c.*2316G>A ENSP00000503806.1:n.*2316G>A
ENST00000678833.1:c.*1902G>A ENSP00000503893.1:n.*1902G>A
ENST00000679023.1:c.1988G>A ENSP00000503718.1:p.Ser663Asn
ENST00000679076.1:c.1769G>A
ENST00000679111.1:c.*906G>A ENSP00000504257.1:n.*906G>A
ENST00000679189.1:c.1799G>A ENSP00000503356.1:p.Ser600Asn
ENST00000341012.11:c.1988G>A ENSP00000343034.7:p.Ser663Asn
ENST00000372220.4:c.1013G>A ENSP00000361294.4:p.Ser338Asn
ENST00000372228.7:c.2216G>A ENSP00000361302.3:p.Ser739Asn
ENST00000402686.7:c.2150G>A ENSP00000385797.3:p.Ser717Asn
ENST00000404875.6:c.1799G>A ENSP00000384531.2:p.Ser600Asn
ENST00000423007.5:c.2150G>A ENSP00000404119.1:p.Ser717Asn
ENST00000485278.5:n.2700G>A
NM_001077365.1:c.2150G>A NP_001070833.1:p.Ser717Asn
NM_001077366.1:c.1988G>A NP_001070834.1:p.Ser663Asn
NM_001136113.1:c.2150G>A NP_001129585.1:p.Ser717Asn
NM_001136114.1:c.1799G>A NP_001129586.1:p.Ser600Asn
NM_007171.3:c.2216G>A NP_009102.3:p.Ser739Asn
XM_005272156.1:c.2216G>A XP_005272213.1:p.Ser739Asn
XM_005272158.1:c.2054G>A XP_005272215.1:p.Ser685Asn
XM_005272159.1:c.1865G>A XP_005272216.1:p.Ser622Asn
XM_005272162.1:c.1019G>A XP_005272219.1:p.Ser340Asn
XM_006716932.1:c.1865G>A XP_006716995.1:p.Ser622Asn
XM_011518140.1:c.2069G>A XP_011516442.1:p.Ser690Asn
XM_011518141.1:c.2003G>A XP_011516443.1:p.Ser668Asn
XM_011518142.1:c.1907G>A XP_011516444.1:p.Ser636Asn
XM_011518143.1:c.1901G>A XP_011516445.1:p.Ser634Asn
XM_011518145.1:c.1760G>A XP_011516447.1:p.Ser587Asn
XM_011518147.1:c.1088G>A XP_011516449.1:p.Ser363Asn
XR_929703.1:n.2392G>A
NM_001353193.1:c.2216G>A NP_001340122.1:p.Ser739Asn
NM_001353194.1:c.1988G>A NP_001340123.1:p.Ser663Asn
NM_001353195.1:c.1799G>A NP_001340124.1:p.Ser600Asn
NM_001353196.1:c.2060G>A NP_001340125.1:p.Ser687Asn
NM_001353197.1:c.2054G>A NP_001340126.1:p.Ser685Asn
NM_001353198.1:c.2054G>A NP_001340127.1:p.Ser685Asn
NM_001353199.1:c.1865G>A NP_001340128.1:p.Ser622Asn
NM_001353200.1:c.1694G>A NP_001340129.1:p.Ser565Asn
NR_148391.1:n.2200G>A
NR_148392.1:n.2418G>A
NR_148393.1:n.2339G>A
NR_148394.1:n.2093G>A
NR_148395.1:n.2491G>A
NR_148396.1:n.2125G>A
NR_148397.1:n.2250G>A
NR_148398.1:n.2205G>A
NR_148399.1:n.2731G>A
NR_148400.1:n.2330G>A
XM_005272162.3:c.1019G>A XP_005272219.1:p.Ser340Asn
XM_006716932.2:c.1865G>A XP_006716995.1:p.Ser622Asn
XM_011518140.2:c.2069G>A XP_011516442.1:p.Ser690Asn
XM_011518141.2:c.2003G>A XP_011516443.1:p.Ser668Asn
XM_011518142.2:c.1907G>A XP_011516444.1:p.Ser636Asn
XM_011518143.2:c.1901G>A XP_011516445.1:p.Ser634Asn
XM_011518145.2:c.1760G>A XP_011516447.1:p.Ser587Asn
XM_017014205.2:c.1019G>A XP_016869694.1:p.Ser340Asn
XM_024447380.1:c.1019G>A XP_024303148.1:p.Ser340Asn
XM_024447381.1:c.1325G>A XP_024303149.1:p.Ser442Asn
XM_024447382.1:c.1019G>A XP_024303150.1:p.Ser340Asn
XR_001746160.2:n.2320G>A
XR_001746162.2:n.2525G>A
XR_001746164.1:n.2242G>A
XR_001746166.2:n.2537G>A
NM_001077365.2:c.2150G>A MANE Select NP_001070833.1:p.Ser717Asn
NM_001077366.2:c.1988G>A NP_001070834.1:p.Ser663Asn
NM_001136113.2:c.2150G>A NP_001129585.1:p.Ser717Asn
NM_001136114.2:c.1799G>A NP_001129586.1:p.Ser600Asn
NM_001353193.2:c.2216G>A NP_001340122.2:p.Ser739Asn
NM_001353194.2:c.1988G>A NP_001340123.1:p.Ser663Asn
NM_001353195.2:c.1799G>A NP_001340124.1:p.Ser600Asn
NM_001353196.2:c.2060G>A NP_001340125.1:p.Ser687Asn
NM_001353197.2:c.2054G>A NP_001340126.2:p.Ser685Asn
NM_001353198.2:c.2054G>A NP_001340127.2:p.Ser685Asn
NM_001353199.2:c.1865G>A NP_001340128.2:p.Ser622Asn
NM_001353200.2:c.1694G>A NP_001340129.1:p.Ser565Asn
NM_001374689.1:c.2138G>A NP_001361618.1:p.Ser713Asn
NM_001374690.1:c.1931G>A NP_001361619.1:p.Ser644Asn
NM_001374691.1:c.1799G>A NP_001361620.1:p.Ser600Asn
NM_001374692.1:c.1799G>A NP_001361621.1:p.Ser600Asn
NM_001374693.1:c.1799G>A NP_001361622.1:p.Ser600Asn
NM_001374695.1:c.1760G>A NP_001361624.1:p.Ser587Asn
NM_007171.4:c.2216G>A NP_009102.4:p.Ser739Asn
NR_148391.2:n.2184G>A
NR_148392.2:n.2402G>A
NR_148393.2:n.2323G>A
NR_148394.2:n.2077G>A
NR_148395.2:n.2475G>A
NR_148396.2:n.2109G>A
NR_148397.2:n.2234G>A
NR_148398.2:n.2189G>A
NR_148399.2:n.2715G>A
NR_148400.2:n.2314G>A