Canonical Allele Identifier: CA375314391
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522124A>T , CM000671.2:g.131522124A>T GRCh38
NC_000009.11:g.134397511A>T , CM000671.1:g.134397511A>T GRCh37
NC_000009.10:g.133387332A>T NCBI36
NG_008896.1:g.24223A>T
NG_008896.2:g.24223A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1741A>T ENSP00000343034.7:p.Met581Leu
ENST00000404875.7:n.2443A>T
ENST00000423007.6:c.1960A>T ENSP00000404119.2:p.Met654Leu
ENST00000677295.2:c.*2247A>T ENSP00000504346.2:n.*2247A>T
ENST00000678264.2:c.*2086A>T ENSP00000503157.2:n.*2086A>T
ENST00000682070.1:n.2291-78A>T
ENST00000682813.1:n.2307A>T
ENST00000683392.1:n.4573-78A>T
ENST00000683712.1:n.2308A>T
ENST00000683900.1:n.3803A>T
ENST00000684062.1:n.2569A>T
ENST00000684579.1:n.3749A>T
ENST00000684679.1:n.1130A>T
ENST00000341012.12:c.1741A>T ENSP00000343034.7:p.Met581Leu
ENST00000372220.5:c.772A>T ENSP00000361294.5:p.Met258Leu
ENST00000372228.9:c.1969A>T ENSP00000361302.3:p.Met657Leu
ENST00000402686.8:c.1903A>T MANE Select ENSP00000385797.4:p.Met635Leu
ENST00000676640.1:c.1903A>T ENSP00000503281.1:p.Met635Leu
ENST00000676803.1:c.964A>T ENSP00000503093.1:p.Met322Leu
ENST00000676835.1:c.*1118A>T ENSP00000502911.1:n.*1118A>T
ENST00000677029.1:c.1447A>T ENSP00000502936.1:p.Met483Leu
ENST00000677099.1:c.*1613A>T ENSP00000504553.1:n.*1613A>T
ENST00000677216.1:c.1552A>T ENSP00000503772.1:p.Met518Leu
ENST00000677221.1:n.928A>T
ENST00000677295.1:c.*1203-78A>T ENSP00000504346.1:n.*1203-78A>T
ENST00000677444.1:c.1848A>T
ENST00000677586.1:n.1270A>T
ENST00000677626.1:c.1552A>T ENSP00000503552.1:p.Met518Leu
ENST00000677853.1:c.*911A>T ENSP00000503488.1:n.*911A>T
ENST00000678202.1:n.1062A>T
ENST00000678264.1:c.*1280A>T ENSP00000503157.1:n.*1280A>T
ENST00000678303.1:c.1813A>T ENSP00000503696.1:p.Met605Leu
ENST00000678366.1:c.*2152A>T ENSP00000504353.1:n.*2152A>T
ENST00000678546.1:c.*1848A>T ENSP00000503062.1:n.*1848A>T
ENST00000678548.1:c.*2042A>T ENSP00000503934.1:n.*2042A>T
ENST00000678626.1:n.1739A>T
ENST00000678739.1:c.*2147-78A>T ENSP00000503806.1:n.*2147-78A>T
ENST00000678833.1:c.*1655A>T ENSP00000503893.1:n.*1655A>T
ENST00000679023.1:c.1741A>T ENSP00000503718.1:p.Met581Leu
ENST00000679076.1:c.1522A>T
ENST00000679111.1:c.*659A>T ENSP00000504257.1:n.*659A>T
ENST00000679189.1:c.1552A>T ENSP00000503356.1:p.Met518Leu
ENST00000341012.11:c.1741A>T ENSP00000343034.7:p.Met581Leu
ENST00000372220.4:c.766A>T ENSP00000361294.4:p.Met256Leu
ENST00000372228.7:c.1969A>T ENSP00000361302.3:p.Met657Leu
ENST00000402686.7:c.1903A>T ENSP00000385797.3:p.Met635Leu
ENST00000404875.6:c.1552A>T ENSP00000384531.2:p.Met518Leu
ENST00000423007.5:c.1903A>T ENSP00000404119.1:p.Met635Leu
ENST00000485278.5:n.2453A>T
ENST00000494883.1:n.446A>T
NM_001077365.1:c.1903A>T NP_001070833.1:p.Met635Leu
NM_001077366.1:c.1741A>T NP_001070834.1:p.Met581Leu
NM_001136113.1:c.1903A>T NP_001129585.1:p.Met635Leu
NM_001136114.1:c.1552A>T NP_001129586.1:p.Met518Leu
NM_007171.3:c.1969A>T NP_009102.3:p.Met657Leu
XM_005272156.1:c.1969A>T XP_005272213.1:p.Met657Leu
XM_005272158.1:c.1807A>T XP_005272215.1:p.Met603Leu
XM_005272159.1:c.1618A>T XP_005272216.1:p.Met540Leu
XM_005272162.1:c.772A>T XP_005272219.1:p.Met258Leu
XM_006716932.1:c.1618A>T XP_006716995.1:p.Met540Leu
XM_011518140.1:c.1822A>T XP_011516442.1:p.Met608Leu
XM_011518141.1:c.1756A>T XP_011516443.1:p.Met586Leu
XM_011518142.1:c.1660A>T XP_011516444.1:p.Met554Leu
XM_011518143.1:c.1654A>T XP_011516445.1:p.Met552Leu
XM_011518145.1:c.1513A>T XP_011516447.1:p.Met505Leu
XM_011518147.1:c.841A>T XP_011516449.1:p.Met281Leu
XR_929703.1:n.2145A>T
NM_001353193.1:c.1969A>T NP_001340122.1:p.Met657Leu
NM_001353194.1:c.1741A>T NP_001340123.1:p.Met581Leu
NM_001353195.1:c.1552A>T NP_001340124.1:p.Met518Leu
NM_001353196.1:c.1813A>T NP_001340125.1:p.Met605Leu
NM_001353197.1:c.1807A>T NP_001340126.1:p.Met603Leu
NM_001353198.1:c.1807A>T NP_001340127.1:p.Met603Leu
NM_001353199.1:c.1618A>T NP_001340128.1:p.Met540Leu
NM_001353200.1:c.1447A>T NP_001340129.1:p.Met483Leu
NR_148391.1:n.1953A>T
NR_148392.1:n.2171A>T
NR_148393.1:n.2092A>T
NR_148394.1:n.1846A>T
NR_148395.1:n.2244A>T
NR_148396.1:n.1878A>T
NR_148397.1:n.2003A>T
NR_148398.1:n.1958A>T
NR_148399.1:n.2484A>T
NR_148400.1:n.2083A>T
XM_005272162.3:c.772A>T XP_005272219.1:p.Met258Leu
XM_006716932.2:c.1618A>T XP_006716995.1:p.Met540Leu
XM_011518140.2:c.1822A>T XP_011516442.1:p.Met608Leu
XM_011518141.2:c.1756A>T XP_011516443.1:p.Met586Leu
XM_011518142.2:c.1660A>T XP_011516444.1:p.Met554Leu
XM_011518143.2:c.1654A>T XP_011516445.1:p.Met552Leu
XM_011518145.2:c.1513A>T XP_011516447.1:p.Met505Leu
XM_017014205.2:c.772A>T XP_016869694.1:p.Met258Leu
XM_024447380.1:c.772A>T XP_024303148.1:p.Met258Leu
XM_024447381.1:c.1078A>T XP_024303149.1:p.Met360Leu
XM_024447382.1:c.772A>T XP_024303150.1:p.Met258Leu
XR_001746160.2:n.2073A>T
XR_001746162.2:n.2278A>T
XR_001746164.1:n.1995A>T
XR_001746166.2:n.2290A>T
NM_001077365.2:c.1903A>T MANE Select NP_001070833.1:p.Met635Leu
NM_001077366.2:c.1741A>T NP_001070834.1:p.Met581Leu
NM_001136113.2:c.1903A>T NP_001129585.1:p.Met635Leu
NM_001136114.2:c.1552A>T NP_001129586.1:p.Met518Leu
NM_001353193.2:c.1969A>T NP_001340122.2:p.Met657Leu
NM_001353194.2:c.1741A>T NP_001340123.1:p.Met581Leu
NM_001353195.2:c.1552A>T NP_001340124.1:p.Met518Leu
NM_001353196.2:c.1813A>T NP_001340125.1:p.Met605Leu
NM_001353197.2:c.1807A>T NP_001340126.2:p.Met603Leu
NM_001353198.2:c.1807A>T NP_001340127.2:p.Met603Leu
NM_001353199.2:c.1618A>T NP_001340128.2:p.Met540Leu
NM_001353200.2:c.1447A>T NP_001340129.1:p.Met483Leu
NM_001374689.1:c.1891A>T NP_001361618.1:p.Met631Leu
NM_001374690.1:c.1684A>T NP_001361619.1:p.Met562Leu
NM_001374691.1:c.1552A>T NP_001361620.1:p.Met518Leu
NM_001374692.1:c.1552A>T NP_001361621.1:p.Met518Leu
NM_001374693.1:c.1552A>T NP_001361622.1:p.Met518Leu
NM_001374695.1:c.1513A>T NP_001361624.1:p.Met505Leu
NM_007171.4:c.1969A>T NP_009102.4:p.Met657Leu
NR_148391.2:n.1937A>T
NR_148392.2:n.2155A>T
NR_148393.2:n.2076A>T
NR_148394.2:n.1830A>T
NR_148395.2:n.2228A>T
NR_148396.2:n.1862A>T
NR_148397.2:n.1987A>T
NR_148398.2:n.1942A>T
NR_148399.2:n.2468A>T
NR_148400.2:n.2067A>T