Canonical Allele Identifier: CA375315068
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522979A>T , CM000671.2:g.131522979A>T GRCh38
NC_000009.11:g.134398366A>T , CM000671.1:g.134398366A>T GRCh37
NC_000009.10:g.133388187A>T NCBI36
NG_008896.1:g.25078A>T
NG_008896.2:g.25078A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000341012.13:c.1889A>T ENSP00000343034.7:p.Tyr630Phe
ENST00000404875.7:n.2591A>T
ENST00000423007.6:c.2108A>T ENSP00000404119.2:p.Tyr703Phe
ENST00000677295.2:c.*2395A>T ENSP00000504346.2:n.*2395A>T
ENST00000678264.2:c.*2234A>T ENSP00000503157.2:n.*2234A>T
ENST00000682070.1:n.2361A>T
ENST00000682639.1:c.48A>T
ENST00000682813.1:n.2448A>T
ENST00000683231.1:c.48A>T
ENST00000683392.1:n.4643A>T
ENST00000683712.1:n.2456A>T
ENST00000683900.1:n.3951A>T
ENST00000684062.1:n.2717A>T
ENST00000684399.1:c.48A>T
ENST00000684579.1:n.3897A>T
ENST00000341012.12:c.1889A>T ENSP00000343034.7:p.Tyr630Phe
ENST00000372220.5:c.920A>T ENSP00000361294.5:p.Tyr307Phe
ENST00000372228.9:c.2117A>T ENSP00000361302.3:p.Tyr706Phe
ENST00000402686.8:c.2051A>T MANE Select ENSP00000385797.4:p.Tyr684Phe
ENST00000676640.1:c.2051A>T ENSP00000503281.1:p.Tyr684Phe
ENST00000676803.1:c.1112A>T ENSP00000503093.1:p.Tyr371Phe
ENST00000676835.1:c.*1266A>T ENSP00000502911.1:n.*1266A>T
ENST00000677029.1:c.1595A>T ENSP00000502936.1:p.Tyr532Phe
ENST00000677099.1:c.*1761A>T ENSP00000504553.1:n.*1761A>T
ENST00000677216.1:c.1700A>T ENSP00000503772.1:p.Tyr567Phe
ENST00000677221.1:n.1076A>T
ENST00000677295.1:c.*1273A>T ENSP00000504346.1:n.*1273A>T
ENST00000677444.1:c.1996A>T
ENST00000677586.1:n.1418A>T
ENST00000677626.1:c.1700A>T ENSP00000503552.1:p.Tyr567Phe
ENST00000677853.1:c.*1059A>T ENSP00000503488.1:n.*1059A>T
ENST00000678264.1:c.*1428A>T ENSP00000503157.1:n.*1428A>T
ENST00000678303.1:c.1961A>T ENSP00000503696.1:p.Tyr654Phe
ENST00000678366.1:c.*2300A>T ENSP00000504353.1:n.*2300A>T
ENST00000678546.1:c.*1996A>T ENSP00000503062.1:n.*1996A>T
ENST00000678548.1:c.*2190A>T ENSP00000503934.1:n.*2190A>T
ENST00000678626.1:n.1887A>T
ENST00000678739.1:c.*2217A>T ENSP00000503806.1:n.*2217A>T
ENST00000678833.1:c.*1803A>T ENSP00000503893.1:n.*1803A>T
ENST00000679023.1:c.1889A>T ENSP00000503718.1:p.Tyr630Phe
ENST00000679076.1:c.1670A>T
ENST00000679111.1:c.*807A>T ENSP00000504257.1:n.*807A>T
ENST00000679189.1:c.1700A>T ENSP00000503356.1:p.Tyr567Phe
ENST00000341012.11:c.1889A>T ENSP00000343034.7:p.Tyr630Phe
ENST00000372220.4:c.914A>T ENSP00000361294.4:p.Tyr305Phe
ENST00000372228.7:c.2117A>T ENSP00000361302.3:p.Tyr706Phe
ENST00000402686.7:c.2051A>T ENSP00000385797.3:p.Tyr684Phe
ENST00000404875.6:c.1700A>T ENSP00000384531.2:p.Tyr567Phe
ENST00000423007.5:c.2051A>T ENSP00000404119.1:p.Tyr684Phe
ENST00000485278.5:n.2601A>T
NM_001077365.1:c.2051A>T NP_001070833.1:p.Tyr684Phe
NM_001077366.1:c.1889A>T NP_001070834.1:p.Tyr630Phe
NM_001136113.1:c.2051A>T NP_001129585.1:p.Tyr684Phe
NM_001136114.1:c.1700A>T NP_001129586.1:p.Tyr567Phe
NM_007171.3:c.2117A>T NP_009102.3:p.Tyr706Phe
XM_005272156.1:c.2117A>T XP_005272213.1:p.Tyr706Phe
XM_005272158.1:c.1955A>T XP_005272215.1:p.Tyr652Phe
XM_005272159.1:c.1766A>T XP_005272216.1:p.Tyr589Phe
XM_005272162.1:c.920A>T XP_005272219.1:p.Tyr307Phe
XM_006716932.1:c.1766A>T XP_006716995.1:p.Tyr589Phe
XM_011518140.1:c.1970A>T XP_011516442.1:p.Tyr657Phe
XM_011518141.1:c.1904A>T XP_011516443.1:p.Tyr635Phe
XM_011518142.1:c.1808A>T XP_011516444.1:p.Tyr603Phe
XM_011518143.1:c.1802A>T XP_011516445.1:p.Tyr601Phe
XM_011518145.1:c.1661A>T XP_011516447.1:p.Tyr554Phe
XM_011518147.1:c.989A>T XP_011516449.1:p.Tyr330Phe
XR_929703.1:n.2293A>T
NM_001353193.1:c.2117A>T NP_001340122.1:p.Tyr706Phe
NM_001353194.1:c.1889A>T NP_001340123.1:p.Tyr630Phe
NM_001353195.1:c.1700A>T NP_001340124.1:p.Tyr567Phe
NM_001353196.1:c.1961A>T NP_001340125.1:p.Tyr654Phe
NM_001353197.1:c.1955A>T NP_001340126.1:p.Tyr652Phe
NM_001353198.1:c.1955A>T NP_001340127.1:p.Tyr652Phe
NM_001353199.1:c.1766A>T NP_001340128.1:p.Tyr589Phe
NM_001353200.1:c.1595A>T NP_001340129.1:p.Tyr532Phe
NR_148391.1:n.2101A>T
NR_148392.1:n.2319A>T
NR_148393.1:n.2240A>T
NR_148394.1:n.1994A>T
NR_148395.1:n.2392A>T
NR_148396.1:n.2026A>T
NR_148397.1:n.2151A>T
NR_148398.1:n.2106A>T
NR_148399.1:n.2632A>T
NR_148400.1:n.2231A>T
XM_005272162.3:c.920A>T XP_005272219.1:p.Tyr307Phe
XM_006716932.2:c.1766A>T XP_006716995.1:p.Tyr589Phe
XM_011518140.2:c.1970A>T XP_011516442.1:p.Tyr657Phe
XM_011518141.2:c.1904A>T XP_011516443.1:p.Tyr635Phe
XM_011518142.2:c.1808A>T XP_011516444.1:p.Tyr603Phe
XM_011518143.2:c.1802A>T XP_011516445.1:p.Tyr601Phe
XM_011518145.2:c.1661A>T XP_011516447.1:p.Tyr554Phe
XM_017014205.2:c.920A>T XP_016869694.1:p.Tyr307Phe
XM_024447380.1:c.920A>T XP_024303148.1:p.Tyr307Phe
XM_024447381.1:c.1226A>T XP_024303149.1:p.Tyr409Phe
XM_024447382.1:c.920A>T XP_024303150.1:p.Tyr307Phe
XR_001746160.2:n.2221A>T
XR_001746162.2:n.2426A>T
XR_001746164.1:n.2143A>T
XR_001746166.2:n.2438A>T
NM_001077365.2:c.2051A>T MANE Select NP_001070833.1:p.Tyr684Phe
NM_001077366.2:c.1889A>T NP_001070834.1:p.Tyr630Phe
NM_001136113.2:c.2051A>T NP_001129585.1:p.Tyr684Phe
NM_001136114.2:c.1700A>T NP_001129586.1:p.Tyr567Phe
NM_001353193.2:c.2117A>T NP_001340122.2:p.Tyr706Phe
NM_001353194.2:c.1889A>T NP_001340123.1:p.Tyr630Phe
NM_001353195.2:c.1700A>T NP_001340124.1:p.Tyr567Phe
NM_001353196.2:c.1961A>T NP_001340125.1:p.Tyr654Phe
NM_001353197.2:c.1955A>T NP_001340126.2:p.Tyr652Phe
NM_001353198.2:c.1955A>T NP_001340127.2:p.Tyr652Phe
NM_001353199.2:c.1766A>T NP_001340128.2:p.Tyr589Phe
NM_001353200.2:c.1595A>T NP_001340129.1:p.Tyr532Phe
NM_001374689.1:c.2039A>T NP_001361618.1:p.Tyr680Phe
NM_001374690.1:c.1832A>T NP_001361619.1:p.Tyr611Phe
NM_001374691.1:c.1700A>T NP_001361620.1:p.Tyr567Phe
NM_001374692.1:c.1700A>T NP_001361621.1:p.Tyr567Phe
NM_001374693.1:c.1700A>T NP_001361622.1:p.Tyr567Phe
NM_001374695.1:c.1661A>T NP_001361624.1:p.Tyr554Phe
NM_007171.4:c.2117A>T NP_009102.4:p.Tyr706Phe
NR_148391.2:n.2085A>T
NR_148392.2:n.2303A>T
NR_148393.2:n.2224A>T
NR_148394.2:n.1978A>T
NR_148395.2:n.2376A>T
NR_148396.2:n.2010A>T
NR_148397.2:n.2135A>T
NR_148398.2:n.2090A>T
NR_148399.2:n.2616A>T
NR_148400.2:n.2215A>T