Canonical Allele Identifier: CA375315026
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522969G>A , CM000671.2:g.131522969G>A GRCh38
NC_000009.11:g.134398356G>A , CM000671.1:g.134398356G>A GRCh37
NC_000009.10:g.133388177G>A NCBI36
NG_008896.1:g.25068G>A
NG_008896.2:g.25068G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1879G>A ENSP00000343034.7:p.Val627Met
ENST00000404875.7:n.2581G>A
ENST00000423007.6:c.2098G>A ENSP00000404119.2:p.Val700Met
ENST00000677295.2:c.*2385G>A ENSP00000504346.2:n.*2385G>A
ENST00000678264.2:c.*2224G>A ENSP00000503157.2:n.*2224G>A
ENST00000682070.1:n.2351G>A
ENST00000682639.1:c.38G>A
ENST00000682813.1:n.2438G>A
ENST00000683231.1:c.38G>A
ENST00000683392.1:n.4633G>A
ENST00000683712.1:n.2446G>A
ENST00000683900.1:n.3941G>A
ENST00000684062.1:n.2707G>A
ENST00000684399.1:c.38G>A
ENST00000684579.1:n.3887G>A
ENST00000341012.12:c.1879G>A ENSP00000343034.7:p.Val627Met
ENST00000372220.5:c.910G>A ENSP00000361294.5:p.Val304Met
ENST00000372228.9:c.2107G>A ENSP00000361302.3:p.Val703Met
ENST00000402686.8:c.2041G>A MANE Select ENSP00000385797.4:p.Val681Met
ENST00000676640.1:c.2041G>A ENSP00000503281.1:p.Val681Met
ENST00000676803.1:c.1102G>A ENSP00000503093.1:p.Val368Met
ENST00000676835.1:c.*1256G>A ENSP00000502911.1:n.*1256G>A
ENST00000677029.1:c.1585G>A ENSP00000502936.1:p.Val529Met
ENST00000677099.1:c.*1751G>A ENSP00000504553.1:n.*1751G>A
ENST00000677216.1:c.1690G>A ENSP00000503772.1:p.Val564Met
ENST00000677221.1:n.1066G>A
ENST00000677295.1:c.*1263G>A ENSP00000504346.1:n.*1263G>A
ENST00000677444.1:c.1986G>A
ENST00000677586.1:n.1408G>A
ENST00000677626.1:c.1690G>A ENSP00000503552.1:p.Val564Met
ENST00000677853.1:c.*1049G>A ENSP00000503488.1:n.*1049G>A
ENST00000678264.1:c.*1418G>A ENSP00000503157.1:n.*1418G>A
ENST00000678303.1:c.1951G>A ENSP00000503696.1:p.Val651Met
ENST00000678366.1:c.*2290G>A ENSP00000504353.1:n.*2290G>A
ENST00000678546.1:c.*1986G>A ENSP00000503062.1:n.*1986G>A
ENST00000678548.1:c.*2180G>A ENSP00000503934.1:n.*2180G>A
ENST00000678626.1:n.1877G>A
ENST00000678739.1:c.*2207G>A ENSP00000503806.1:n.*2207G>A
ENST00000678833.1:c.*1793G>A ENSP00000503893.1:n.*1793G>A
ENST00000679023.1:c.1879G>A ENSP00000503718.1:p.Val627Met
ENST00000679076.1:c.1660G>A
ENST00000679111.1:c.*797G>A ENSP00000504257.1:n.*797G>A
ENST00000679189.1:c.1690G>A ENSP00000503356.1:p.Val564Met
ENST00000341012.11:c.1879G>A ENSP00000343034.7:p.Val627Met
ENST00000372220.4:c.904G>A ENSP00000361294.4:p.Val302Met
ENST00000372228.7:c.2107G>A ENSP00000361302.3:p.Val703Met
ENST00000402686.7:c.2041G>A ENSP00000385797.3:p.Val681Met
ENST00000404875.6:c.1690G>A ENSP00000384531.2:p.Val564Met
ENST00000423007.5:c.2041G>A ENSP00000404119.1:p.Val681Met
ENST00000485278.5:n.2591G>A
NM_001077365.1:c.2041G>A NP_001070833.1:p.Val681Met
NM_001077366.1:c.1879G>A NP_001070834.1:p.Val627Met
NM_001136113.1:c.2041G>A NP_001129585.1:p.Val681Met
NM_001136114.1:c.1690G>A NP_001129586.1:p.Val564Met
NM_007171.3:c.2107G>A NP_009102.3:p.Val703Met
XM_005272156.1:c.2107G>A XP_005272213.1:p.Val703Met
XM_005272158.1:c.1945G>A XP_005272215.1:p.Val649Met
XM_005272159.1:c.1756G>A XP_005272216.1:p.Val586Met
XM_005272162.1:c.910G>A XP_005272219.1:p.Val304Met
XM_006716932.1:c.1756G>A XP_006716995.1:p.Val586Met
XM_011518140.1:c.1960G>A XP_011516442.1:p.Val654Met
XM_011518141.1:c.1894G>A XP_011516443.1:p.Val632Met
XM_011518142.1:c.1798G>A XP_011516444.1:p.Val600Met
XM_011518143.1:c.1792G>A XP_011516445.1:p.Val598Met
XM_011518145.1:c.1651G>A XP_011516447.1:p.Val551Met
XM_011518147.1:c.979G>A XP_011516449.1:p.Val327Met
XR_929703.1:n.2283G>A
NM_001353193.1:c.2107G>A NP_001340122.1:p.Val703Met
NM_001353194.1:c.1879G>A NP_001340123.1:p.Val627Met
NM_001353195.1:c.1690G>A NP_001340124.1:p.Val564Met
NM_001353196.1:c.1951G>A NP_001340125.1:p.Val651Met
NM_001353197.1:c.1945G>A NP_001340126.1:p.Val649Met
NM_001353198.1:c.1945G>A NP_001340127.1:p.Val649Met
NM_001353199.1:c.1756G>A NP_001340128.1:p.Val586Met
NM_001353200.1:c.1585G>A NP_001340129.1:p.Val529Met
NR_148391.1:n.2091G>A
NR_148392.1:n.2309G>A
NR_148393.1:n.2230G>A
NR_148394.1:n.1984G>A
NR_148395.1:n.2382G>A
NR_148396.1:n.2016G>A
NR_148397.1:n.2141G>A
NR_148398.1:n.2096G>A
NR_148399.1:n.2622G>A
NR_148400.1:n.2221G>A
XM_005272162.3:c.910G>A XP_005272219.1:p.Val304Met
XM_006716932.2:c.1756G>A XP_006716995.1:p.Val586Met
XM_011518140.2:c.1960G>A XP_011516442.1:p.Val654Met
XM_011518141.2:c.1894G>A XP_011516443.1:p.Val632Met
XM_011518142.2:c.1798G>A XP_011516444.1:p.Val600Met
XM_011518143.2:c.1792G>A XP_011516445.1:p.Val598Met
XM_011518145.2:c.1651G>A XP_011516447.1:p.Val551Met
XM_017014205.2:c.910G>A XP_016869694.1:p.Val304Met
XM_024447380.1:c.910G>A XP_024303148.1:p.Val304Met
XM_024447381.1:c.1216G>A XP_024303149.1:p.Val406Met
XM_024447382.1:c.910G>A XP_024303150.1:p.Val304Met
XR_001746160.2:n.2211G>A
XR_001746162.2:n.2416G>A
XR_001746164.1:n.2133G>A
XR_001746166.2:n.2428G>A
NM_001077365.2:c.2041G>A MANE Select NP_001070833.1:p.Val681Met
NM_001077366.2:c.1879G>A NP_001070834.1:p.Val627Met
NM_001136113.2:c.2041G>A NP_001129585.1:p.Val681Met
NM_001136114.2:c.1690G>A NP_001129586.1:p.Val564Met
NM_001353193.2:c.2107G>A NP_001340122.2:p.Val703Met
NM_001353194.2:c.1879G>A NP_001340123.1:p.Val627Met
NM_001353195.2:c.1690G>A NP_001340124.1:p.Val564Met
NM_001353196.2:c.1951G>A NP_001340125.1:p.Val651Met
NM_001353197.2:c.1945G>A NP_001340126.2:p.Val649Met
NM_001353198.2:c.1945G>A NP_001340127.2:p.Val649Met
NM_001353199.2:c.1756G>A NP_001340128.2:p.Val586Met
NM_001353200.2:c.1585G>A NP_001340129.1:p.Val529Met
NM_001374689.1:c.2029G>A NP_001361618.1:p.Val677Met
NM_001374690.1:c.1822G>A NP_001361619.1:p.Val608Met
NM_001374691.1:c.1690G>A NP_001361620.1:p.Val564Met
NM_001374692.1:c.1690G>A NP_001361621.1:p.Val564Met
NM_001374693.1:c.1690G>A NP_001361622.1:p.Val564Met
NM_001374695.1:c.1651G>A NP_001361624.1:p.Val551Met
NM_007171.4:c.2107G>A NP_009102.4:p.Val703Met
NR_148391.2:n.2075G>A
NR_148392.2:n.2293G>A
NR_148393.2:n.2214G>A
NR_148394.2:n.1968G>A
NR_148395.2:n.2366G>A
NR_148396.2:n.2000G>A
NR_148397.2:n.2125G>A
NR_148398.2:n.2080G>A
NR_148399.2:n.2606G>A
NR_148400.2:n.2205G>A