Canonical Allele Identifier: CA1881760734

Gene: POMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131523145G= , CM000671.2:g.131523145G=	GRCh38
NC_000009.11:g.134398532G= , CM000671.1:g.134398532G=	GRCh37
NC_000009.10:g.133388353G=	NCBI36
NG_008896.1:g.25244G=
NG_008896.2:g.25244G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.*39G=	ENSP00000343034.7:n.*39G=
ENST00000404875.7:n.2757G=
ENST00000677295.2:c.*2561G=	ENSP00000504346.2:n.*2561G=
ENST00000678264.2:c.*2400G=	ENSP00000503157.2:n.*2400G=
ENST00000682070.1:n.2527G=
ENST00000682639.1:c.214G=
ENST00000682813.1:n.2614G=
ENST00000683231.1:c.214G=
ENST00000683392.1:n.4809G=
ENST00000683900.1:n.4117G=
ENST00000684062.1:n.2883G=
ENST00000684399.1:c.214G=
ENST00000684579.1:n.4063G=
ENST00000341012.12:c.*39G=	ENSP00000343034.7:n.*39G=
ENST00000372220.5:c.*39G=	ENSP00000361294.5:n.*39G=
ENST00000372228.9:c.*39G=	ENSP00000361302.3:n.*39G=
ENST00000402686.8:c.*39G= MANE Select	ENSP00000385797.4:n.*39G=
ENST00000676640.1:c.*39G=	ENSP00000503281.1:n.*39G=
ENST00000676803.1:c.*39G=	ENSP00000503093.1:n.*39G=
ENST00000676835.1:c.*1432G=	ENSP00000502911.1:n.*1432G=
ENST00000677029.1:c.*39G=	ENSP00000502936.1:n.*39G=
ENST00000677099.1:c.*1927G=	ENSP00000504553.1:n.*1927G=
ENST00000677216.1:c.*39G=	ENSP00000503772.1:n.*39G=
ENST00000677295.1:c.*1439G=	ENSP00000504346.1:n.*1439G=
ENST00000677444.1:c.2162G=
ENST00000677586.1:n.1584G=
ENST00000677626.1:c.*39G=	ENSP00000503552.1:n.*39G=
ENST00000677853.1:c.*1225G=	ENSP00000503488.1:n.*1225G=
ENST00000678303.1:c.*39G=	ENSP00000503696.1:n.*39G=
ENST00000678366.1:c.*2466G=	ENSP00000504353.1:n.*2466G=
ENST00000678546.1:c.*2162G=	ENSP00000503062.1:n.*2162G=
ENST00000678548.1:c.*2356G=	ENSP00000503934.1:n.*2356G=
ENST00000678626.1:n.2053G=
ENST00000678739.1:c.*2383G=	ENSP00000503806.1:n.*2383G=
ENST00000678833.1:c.*1969G=	ENSP00000503893.1:n.*1969G=
ENST00000679023.1:c.*39G=	ENSP00000503718.1:n.*39G=
ENST00000679076.1:c.1836G=
ENST00000679111.1:c.*973G=	ENSP00000504257.1:n.*973G=
ENST00000679189.1:c.*39G=	ENSP00000503356.1:n.*39G=
ENST00000341012.11:c.*39G=	ENSP00000343034.7:n.*39G=
ENST00000372220.4:c.1080G=	ENSP00000361294.4:n.1080G=
ENST00000372228.7:c.*39G=	ENSP00000361302.3:n.*39G=
ENST00000402686.7:c.*39G=	ENSP00000385797.3:n.*39G=
ENST00000404875.6:c.*39G=	ENSP00000384531.2:n.*39G=
ENST00000423007.5:c.*39G=	ENSP00000404119.1:n.*39G=
ENST00000485278.5:n.2767G=
NM_001077365.1:c.*39G=	NP_001070833.1:n.*39G=
NM_001077366.1:c.*39G=	NP_001070834.1:n.*39G=
NM_001136113.1:c.*39G=	NP_001129585.1:n.*39G=
NM_001136114.1:c.*39G=	NP_001129586.1:n.*39G=
NM_007171.3:c.*39G=	NP_009102.3:n.*39G=
XM_005272156.1:c.*39G=	XP_005272213.1:n.*39G=
XM_005272158.1:c.*39G=	XP_005272215.1:n.*39G=
XM_005272159.1:c.*39G=	XP_005272216.1:n.*39G=
XM_005272162.1:c.*39G=	XP_005272219.1:n.*39G=
XM_006716932.1:c.*39G=	XP_006716995.1:n.*39G=
XM_011518140.1:c.*39G=	XP_011516442.1:n.*39G=
XM_011518141.1:c.*39G=	XP_011516443.1:n.*39G=
XM_011518142.1:c.*39G=	XP_011516444.1:n.*39G=
XM_011518143.1:c.*39G=	XP_011516445.1:n.*39G=
XM_011518145.1:c.*39G=	XP_011516447.1:n.*39G=
XM_011518147.1:c.*39G=	XP_011516449.1:n.*39G=
XR_929703.1:n.2459G=
NM_001353193.1:c.*39G=	NP_001340122.1:n.*39G=
NM_001353194.1:c.*39G=	NP_001340123.1:n.*39G=
NM_001353195.1:c.*39G=	NP_001340124.1:n.*39G=
NM_001353196.1:c.*39G=	NP_001340125.1:n.*39G=
NM_001353197.1:c.*39G=	NP_001340126.1:n.*39G=
NM_001353198.1:c.*39G=	NP_001340127.1:n.*39G=
NM_001353199.1:c.*39G=	NP_001340128.1:n.*39G=
NM_001353200.1:c.*39G=	NP_001340129.1:n.*39G=
NR_148391.1:n.2267G=
NR_148392.1:n.2485G=
NR_148393.1:n.2406G=
NR_148394.1:n.2160G=
NR_148395.1:n.2558G=
NR_148396.1:n.2192G=
NR_148397.1:n.2317G=
NR_148398.1:n.2272G=
NR_148399.1:n.2798G=
NR_148400.1:n.2397G=
XM_005272162.3:c.*39G=	XP_005272219.1:n.*39G=
XM_006716932.2:c.*39G=	XP_006716995.1:n.*39G=
XM_011518140.2:c.*39G=	XP_011516442.1:n.*39G=
XM_011518141.2:c.*39G=	XP_011516443.1:n.*39G=
XM_011518142.2:c.*39G=	XP_011516444.1:n.*39G=
XM_011518143.2:c.*39G=	XP_011516445.1:n.*39G=
XM_011518145.2:c.*39G=	XP_011516447.1:n.*39G=
XM_017014205.2:c.*39G=	XP_016869694.1:n.*39G=
XM_024447380.1:c.*39G=	XP_024303148.1:n.*39G=
XM_024447381.1:c.*39G=	XP_024303149.1:n.*39G=
XM_024447382.1:c.*39G=	XP_024303150.1:n.*39G=
XR_001746160.2:n.2387G=
XR_001746162.2:n.2592G=
XR_001746164.1:n.2309G=
XR_001746166.2:n.2604G=
NM_001077365.2:c.*39G= MANE Select	NP_001070833.1:n.*39G=
NM_001077366.2:c.*39G=	NP_001070834.1:n.*39G=
NM_001136113.2:c.*39G=	NP_001129585.1:n.*39G=
NM_001136114.2:c.*39G=	NP_001129586.1:n.*39G=
NM_001353193.2:c.*39G=	NP_001340122.2:n.*39G=
NM_001353194.2:c.*39G=	NP_001340123.1:n.*39G=
NM_001353195.2:c.*39G=	NP_001340124.1:n.*39G=
NM_001353196.2:c.*39G=	NP_001340125.1:n.*39G=
NM_001353197.2:c.*39G=	NP_001340126.2:n.*39G=
NM_001353198.2:c.*39G=	NP_001340127.2:n.*39G=
NM_001353199.2:c.*39G=	NP_001340128.2:n.*39G=
NM_001353200.2:c.*39G=	NP_001340129.1:n.*39G=
NM_001374689.1:c.*39G=	NP_001361618.1:n.*39G=
NM_001374690.1:c.*39G=	NP_001361619.1:n.*39G=
NM_001374691.1:c.*39G=	NP_001361620.1:n.*39G=
NM_001374692.1:c.*39G=	NP_001361621.1:n.*39G=
NM_001374693.1:c.*39G=	NP_001361622.1:n.*39G=
NM_001374695.1:c.*39G=	NP_001361624.1:n.*39G=
NM_007171.4:c.*39G=	NP_009102.4:n.*39G=
NR_148391.2:n.2251G=
NR_148392.2:n.2469G=
NR_148393.2:n.2390G=
NR_148394.2:n.2144G=
NR_148395.2:n.2542G=
NR_148396.2:n.2176G=
NR_148397.2:n.2301G=
NR_148398.2:n.2256G=
NR_148399.2:n.2782G=
NR_148400.2:n.2381G=