Canonical Allele Identifier: CA467424016

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134397456G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522069G>T , CM000671.2:g.131522069G>T	GRCh38
NC_000009.11:g.134397456G>T , CM000671.1:g.134397456G>T	GRCh37
NC_000009.10:g.133387277G>T	NCBI36
NG_008896.1:g.24168G>T
NG_008896.2:g.24168G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000341012.13:c.1686G>T	ENSP00000343034.7:p.Leu562=
ENST00000404875.7:n.2388G>T
ENST00000423007.6:c.1905G>T	ENSP00000404119.2:p.Leu635=
ENST00000677295.2:c.*2192G>T	ENSP00000504346.2:n.*2192G>T
ENST00000678264.2:c.*2031G>T	ENSP00000503157.2:n.*2031G>T
ENST00000682070.1:n.2291-133G>T
ENST00000682813.1:n.2252G>T
ENST00000683392.1:n.4573-133G>T
ENST00000683712.1:n.2253G>T
ENST00000683900.1:n.3748G>T
ENST00000684062.1:n.2514G>T
ENST00000684579.1:n.3694G>T
ENST00000684679.1:n.1075G>T
ENST00000341012.12:c.1686G>T	ENSP00000343034.7:p.Leu562=
ENST00000372220.5:c.717G>T	ENSP00000361294.5:p.Leu239=
ENST00000372228.9:c.1914G>T	ENSP00000361302.3:p.Leu638=
ENST00000402686.8:c.1848G>T MANE Select	ENSP00000385797.4:p.Leu616=
ENST00000676640.1:c.1848G>T	ENSP00000503281.1:p.Leu616=
ENST00000676803.1:c.909G>T	ENSP00000503093.1:p.Leu303=
ENST00000676835.1:c.*1063G>T	ENSP00000502911.1:n.*1063G>T
ENST00000677029.1:c.1392G>T	ENSP00000502936.1:p.Leu464=
ENST00000677099.1:c.*1558G>T	ENSP00000504553.1:n.*1558G>T
ENST00000677216.1:c.1497G>T	ENSP00000503772.1:p.Leu499=
ENST00000677221.1:n.873G>T
ENST00000677295.1:c.*1203-133G>T	ENSP00000504346.1:n.*1203-133G>T
ENST00000677444.1:c.1793G>T
ENST00000677586.1:n.1215G>T
ENST00000677626.1:c.1497G>T	ENSP00000503552.1:p.Leu499=
ENST00000677853.1:c.*856G>T	ENSP00000503488.1:n.*856G>T
ENST00000678202.1:n.1007G>T
ENST00000678264.1:c.*1225G>T	ENSP00000503157.1:n.*1225G>T
ENST00000678303.1:c.1758G>T	ENSP00000503696.1:p.Leu586=
ENST00000678366.1:c.*2097G>T	ENSP00000504353.1:n.*2097G>T
ENST00000678546.1:c.*1793G>T	ENSP00000503062.1:n.*1793G>T
ENST00000678548.1:c.*1987G>T	ENSP00000503934.1:n.*1987G>T
ENST00000678626.1:n.1684G>T
ENST00000678739.1:c.*2147-133G>T	ENSP00000503806.1:n.*2147-133G>T
ENST00000678833.1:c.*1600G>T	ENSP00000503893.1:n.*1600G>T
ENST00000679023.1:c.1686G>T	ENSP00000503718.1:p.Leu562=
ENST00000679076.1:c.1467G>T
ENST00000679111.1:c.*604G>T	ENSP00000504257.1:n.*604G>T
ENST00000679189.1:c.1497G>T	ENSP00000503356.1:p.Leu499=
ENST00000341012.11:c.1686G>T	ENSP00000343034.7:p.Leu562=
ENST00000372220.4:c.711G>T	ENSP00000361294.4:p.Leu237=
ENST00000372228.7:c.1914G>T	ENSP00000361302.3:p.Leu638=
ENST00000402686.7:c.1848G>T	ENSP00000385797.3:p.Leu616=
ENST00000404875.6:c.1497G>T	ENSP00000384531.2:p.Leu499=
ENST00000423007.5:c.1848G>T	ENSP00000404119.1:p.Leu616=
ENST00000485278.5:n.2398G>T
ENST00000494883.1:n.391G>T
NM_001077365.1:c.1848G>T	NP_001070833.1:p.Leu616=
NM_001077366.1:c.1686G>T	NP_001070834.1:p.Leu562=
NM_001136113.1:c.1848G>T	NP_001129585.1:p.Leu616=
NM_001136114.1:c.1497G>T	NP_001129586.1:p.Leu499=
NM_007171.3:c.1914G>T	NP_009102.3:p.Leu638=
XM_005272156.1:c.1914G>T	XP_005272213.1:p.Leu638=
XM_005272158.1:c.1752G>T	XP_005272215.1:p.Leu584=
XM_005272159.1:c.1563G>T	XP_005272216.1:p.Leu521=
XM_005272162.1:c.717G>T	XP_005272219.1:p.Leu239=
XM_006716932.1:c.1563G>T	XP_006716995.1:p.Leu521=
XM_011518140.1:c.1767G>T	XP_011516442.1:p.Leu589=
XM_011518141.1:c.1701G>T	XP_011516443.1:p.Leu567=
XM_011518142.1:c.1605G>T	XP_011516444.1:p.Leu535=
XM_011518143.1:c.1599G>T	XP_011516445.1:p.Leu533=
XM_011518145.1:c.1458G>T	XP_011516447.1:p.Leu486=
XM_011518147.1:c.786G>T	XP_011516449.1:p.Leu262=
XR_929703.1:n.2090G>T
NM_001353193.1:c.1914G>T	NP_001340122.1:p.Leu638=
NM_001353194.1:c.1686G>T	NP_001340123.1:p.Leu562=
NM_001353195.1:c.1497G>T	NP_001340124.1:p.Leu499=
NM_001353196.1:c.1758G>T	NP_001340125.1:p.Leu586=
NM_001353197.1:c.1752G>T	NP_001340126.1:p.Leu584=
NM_001353198.1:c.1752G>T	NP_001340127.1:p.Leu584=
NM_001353199.1:c.1563G>T	NP_001340128.1:p.Leu521=
NM_001353200.1:c.1392G>T	NP_001340129.1:p.Leu464=
NR_148391.1:n.1898G>T
NR_148392.1:n.2116G>T
NR_148393.1:n.2037G>T
NR_148394.1:n.1791G>T
NR_148395.1:n.2189G>T
NR_148396.1:n.1823G>T
NR_148397.1:n.1948G>T
NR_148398.1:n.1903G>T
NR_148399.1:n.2429G>T
NR_148400.1:n.2028G>T
XM_005272162.3:c.717G>T	XP_005272219.1:p.Leu239=
XM_006716932.2:c.1563G>T	XP_006716995.1:p.Leu521=
XM_011518140.2:c.1767G>T	XP_011516442.1:p.Leu589=
XM_011518141.2:c.1701G>T	XP_011516443.1:p.Leu567=
XM_011518142.2:c.1605G>T	XP_011516444.1:p.Leu535=
XM_011518143.2:c.1599G>T	XP_011516445.1:p.Leu533=
XM_011518145.2:c.1458G>T	XP_011516447.1:p.Leu486=
XM_017014205.2:c.717G>T	XP_016869694.1:p.Leu239=
XM_024447380.1:c.717G>T	XP_024303148.1:p.Leu239=
XM_024447381.1:c.1023G>T	XP_024303149.1:p.Leu341=
XM_024447382.1:c.717G>T	XP_024303150.1:p.Leu239=
XR_001746160.2:n.2018G>T
XR_001746162.2:n.2223G>T
XR_001746164.1:n.1940G>T
XR_001746166.2:n.2235G>T
NM_001077365.2:c.1848G>T MANE Select	NP_001070833.1:p.Leu616=
NM_001077366.2:c.1686G>T	NP_001070834.1:p.Leu562=
NM_001136113.2:c.1848G>T	NP_001129585.1:p.Leu616=
NM_001136114.2:c.1497G>T	NP_001129586.1:p.Leu499=
NM_001353193.2:c.1914G>T	NP_001340122.2:p.Leu638=
NM_001353194.2:c.1686G>T	NP_001340123.1:p.Leu562=
NM_001353195.2:c.1497G>T	NP_001340124.1:p.Leu499=
NM_001353196.2:c.1758G>T	NP_001340125.1:p.Leu586=
NM_001353197.2:c.1752G>T	NP_001340126.2:p.Leu584=
NM_001353198.2:c.1752G>T	NP_001340127.2:p.Leu584=
NM_001353199.2:c.1563G>T	NP_001340128.2:p.Leu521=
NM_001353200.2:c.1392G>T	NP_001340129.1:p.Leu464=
NM_001374689.1:c.1836G>T	NP_001361618.1:p.Leu612=
NM_001374690.1:c.1629G>T	NP_001361619.1:p.Leu543=
NM_001374691.1:c.1497G>T	NP_001361620.1:p.Leu499=
NM_001374692.1:c.1497G>T	NP_001361621.1:p.Leu499=
NM_001374693.1:c.1497G>T	NP_001361622.1:p.Leu499=
NM_001374695.1:c.1458G>T	NP_001361624.1:p.Leu486=
NM_007171.4:c.1914G>T	NP_009102.4:p.Leu638=
NR_148391.2:n.1882G>T
NR_148392.2:n.2100G>T
NR_148393.2:n.2021G>T
NR_148394.2:n.1775G>T
NR_148395.2:n.2173G>T
NR_148396.2:n.1807G>T
NR_148397.2:n.1932G>T
NR_148398.2:n.1887G>T
NR_148399.2:n.2413G>T
NR_148400.2:n.2012G>T