Canonical Allele Identifier: CA10629164
Gene: POMT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 365291
dbSNP Id: rs4740259

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523391A>G , CM000671.2:g.131523391A>G GRCh38
NC_000009.11:g.134398778A>G , CM000671.1:g.134398778A>G GRCh37
NC_000009.10:g.133388599A>G NCBI36
NG_008896.1:g.25490A>G
NG_008896.2:g.25490A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000341012.13:c.*285A>G ENSP00000343034.7:n.*285A>G
ENST00000404875.7:n.3003A>G
ENST00000677295.2:c.*2807A>G ENSP00000504346.2:n.*2807A>G
ENST00000678264.2:c.*2646A>G ENSP00000503157.2:n.*2646A>G
ENST00000682070.1:n.2773A>G
ENST00000682639.1:c.240-72A>G
ENST00000682813.1:n.2860A>G
ENST00000683231.1:c.313A>G
ENST00000683392.1:n.5055A>G
ENST00000683900.1:n.4363A>G
ENST00000684062.1:n.3129A>G
ENST00000684399.1:c.278A>G
ENST00000684579.1:n.4309A>G
ENST00000341012.12:c.*285A>G ENSP00000343034.7:n.*285A>G
ENST00000372220.5:c.*285A>G ENSP00000361294.5:n.*285A>G
ENST00000372228.9:c.*285A>G ENSP00000361302.3:n.*285A>G
ENST00000402686.8:c.*285A>G MANE Select ENSP00000385797.4:n.*285A>G
ENST00000676640.1:c.*285A>G ENSP00000503281.1:n.*285A>G
ENST00000676803.1:c.*285A>G ENSP00000503093.1:n.*285A>G
ENST00000676835.1:c.*1678A>G ENSP00000502911.1:n.*1678A>G
ENST00000677099.1:c.*2173A>G ENSP00000504553.1:n.*2173A>G
ENST00000677216.1:c.*285A>G ENSP00000503772.1:n.*285A>G
ENST00000677295.1:c.*1685A>G ENSP00000504346.1:n.*1685A>G
ENST00000677444.1:c.2408A>G
ENST00000677626.1:c.*285A>G ENSP00000503552.1:n.*285A>G
ENST00000677853.1:c.*1471A>G ENSP00000503488.1:n.*1471A>G
ENST00000678303.1:c.*285A>G ENSP00000503696.1:n.*285A>G
ENST00000678366.1:c.*2712A>G ENSP00000504353.1:n.*2712A>G
ENST00000678546.1:c.*2408A>G ENSP00000503062.1:n.*2408A>G
ENST00000678548.1:c.*2602A>G ENSP00000503934.1:n.*2602A>G
ENST00000678626.1:n.2299A>G
ENST00000678739.1:c.*2629A>G ENSP00000503806.1:n.*2629A>G
ENST00000678833.1:c.*2215A>G ENSP00000503893.1:n.*2215A>G
ENST00000679023.1:c.*109A>G ENSP00000503718.1:n.*109A>G
ENST00000679076.1:c.2082A>G
ENST00000679111.1:c.*1219A>G ENSP00000504257.1:n.*1219A>G
ENST00000341012.11:c.*285A>G ENSP00000343034.7:n.*285A>G
ENST00000372220.4:c.1326A>G ENSP00000361294.4:n.1326A>G
ENST00000372228.7:c.*285A>G ENSP00000361302.3:n.*285A>G
ENST00000402686.7:c.*285A>G ENSP00000385797.3:n.*285A>G
ENST00000404875.6:c.*285A>G ENSP00000384531.2:n.*285A>G
ENST00000423007.5:c.*285A>G ENSP00000404119.1:n.*285A>G
ENST00000485278.5:n.3013A>G
NM_001077365.1:c.*285A>G NP_001070833.1:n.*285A>G
NM_001077366.1:c.*285A>G NP_001070834.1:n.*285A>G
NM_001136113.1:c.*285A>G NP_001129585.1:n.*285A>G
NM_001136114.1:c.*285A>G NP_001129586.1:n.*285A>G
NM_007171.3:c.*285A>G NP_009102.3:n.*285A>G
XM_005272156.1:c.*285A>G XP_005272213.1:n.*285A>G
XM_005272158.1:c.*285A>G XP_005272215.1:n.*285A>G
XM_005272159.1:c.*285A>G XP_005272216.1:n.*285A>G
XM_005272162.1:c.*285A>G XP_005272219.1:n.*285A>G
XM_006716932.1:c.*285A>G XP_006716995.1:n.*285A>G
XM_011518140.1:c.*285A>G XP_011516442.1:n.*285A>G
XM_011518141.1:c.*285A>G XP_011516443.1:n.*285A>G
XM_011518142.1:c.*285A>G XP_011516444.1:n.*285A>G
XM_011518143.1:c.*285A>G XP_011516445.1:n.*285A>G
XM_011518145.1:c.*285A>G XP_011516447.1:n.*285A>G
XM_011518147.1:c.*285A>G XP_011516449.1:n.*285A>G
XR_929703.1:n.2529A>G
NM_001353193.1:c.*285A>G NP_001340122.1:n.*285A>G
NM_001353194.1:c.*285A>G NP_001340123.1:n.*285A>G
NM_001353195.1:c.*285A>G NP_001340124.1:n.*285A>G
NM_001353196.1:c.*285A>G NP_001340125.1:n.*285A>G
NM_001353197.1:c.*285A>G NP_001340126.1:n.*285A>G
NM_001353198.1:c.*285A>G NP_001340127.1:n.*285A>G
NM_001353199.1:c.*285A>G NP_001340128.1:n.*285A>G
NM_001353200.1:c.*285A>G NP_001340129.1:n.*285A>G
NR_148391.1:n.2337A>G
NR_148392.1:n.2555A>G
NR_148393.1:n.2652A>G
NR_148394.1:n.2406A>G
NR_148395.1:n.2804A>G
NR_148396.1:n.2438A>G
NR_148397.1:n.2563A>G
NR_148398.1:n.2518A>G
NR_148399.1:n.2868A>G
NR_148400.1:n.2643A>G
XM_005272162.3:c.*285A>G XP_005272219.1:n.*285A>G
XM_006716932.2:c.*285A>G XP_006716995.1:n.*285A>G
XM_011518140.2:c.*285A>G XP_011516442.1:n.*285A>G
XM_011518141.2:c.*285A>G XP_011516443.1:n.*285A>G
XM_011518142.2:c.*285A>G XP_011516444.1:n.*285A>G
XM_011518143.2:c.*285A>G XP_011516445.1:n.*285A>G
XM_011518145.2:c.*285A>G XP_011516447.1:n.*285A>G
XM_017014205.2:c.*285A>G XP_016869694.1:n.*285A>G
XM_024447380.1:c.*285A>G XP_024303148.1:n.*285A>G
XM_024447381.1:c.*285A>G XP_024303149.1:n.*285A>G
XM_024447382.1:c.*285A>G XP_024303150.1:n.*285A>G
XR_001746160.2:n.2457A>G
XR_001746162.2:n.2838A>G
XR_001746164.1:n.2555A>G
XR_001746166.2:n.2674A>G
NM_001077365.2:c.*285A>G MANE Select NP_001070833.1:n.*285A>G
NM_001077366.2:c.*285A>G NP_001070834.1:n.*285A>G
NM_001136113.2:c.*285A>G NP_001129585.1:n.*285A>G
NM_001136114.2:c.*285A>G NP_001129586.1:n.*285A>G
NM_001353193.2:c.*285A>G NP_001340122.2:n.*285A>G
NM_001353194.2:c.*285A>G NP_001340123.1:n.*285A>G
NM_001353195.2:c.*285A>G NP_001340124.1:n.*285A>G
NM_001353196.2:c.*285A>G NP_001340125.1:n.*285A>G
NM_001353197.2:c.*285A>G NP_001340126.2:n.*285A>G
NM_001353198.2:c.*285A>G NP_001340127.2:n.*285A>G
NM_001353199.2:c.*285A>G NP_001340128.2:n.*285A>G
NM_001353200.2:c.*285A>G NP_001340129.1:n.*285A>G
NM_001374689.1:c.*285A>G NP_001361618.1:n.*285A>G
NM_001374690.1:c.*285A>G NP_001361619.1:n.*285A>G
NM_001374691.1:c.*285A>G NP_001361620.1:n.*285A>G
NM_001374692.1:c.*285A>G NP_001361621.1:n.*285A>G
NM_001374693.1:c.*285A>G NP_001361622.1:n.*285A>G
NM_001374695.1:c.*285A>G NP_001361624.1:n.*285A>G
NM_007171.4:c.*285A>G NP_009102.4:n.*285A>G
NR_148391.2:n.2321A>G
NR_148392.2:n.2539A>G
NR_148393.2:n.2636A>G
NR_148394.2:n.2390A>G
NR_148395.2:n.2788A>G
NR_148396.2:n.2422A>G
NR_148397.2:n.2547A>G
NR_148398.2:n.2502A>G
NR_148399.2:n.2852A>G
NR_148400.2:n.2627A>G