Canonical Allele Identifier: CA467424029

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134397471T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522084T>C , CM000671.2:g.131522084T>C	GRCh38
NC_000009.11:g.134397471T>C , CM000671.1:g.134397471T>C	GRCh37
NC_000009.10:g.133387292T>C	NCBI36
NG_008896.1:g.24183T>C
NG_008896.2:g.24183T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000341012.13:c.1701T>C	ENSP00000343034.7:p.Cys567=
ENST00000404875.7:n.2403T>C
ENST00000423007.6:c.1920T>C	ENSP00000404119.2:p.Cys640=
ENST00000677295.2:c.*2207T>C	ENSP00000504346.2:n.*2207T>C
ENST00000678264.2:c.*2046T>C	ENSP00000503157.2:n.*2046T>C
ENST00000682070.1:n.2291-118T>C
ENST00000682813.1:n.2267T>C
ENST00000683392.1:n.4573-118T>C
ENST00000683712.1:n.2268T>C
ENST00000683900.1:n.3763T>C
ENST00000684062.1:n.2529T>C
ENST00000684579.1:n.3709T>C
ENST00000684679.1:n.1090T>C
ENST00000341012.12:c.1701T>C	ENSP00000343034.7:p.Cys567=
ENST00000372220.5:c.732T>C	ENSP00000361294.5:p.Cys244=
ENST00000372228.9:c.1929T>C	ENSP00000361302.3:p.Cys643=
ENST00000402686.8:c.1863T>C MANE Select	ENSP00000385797.4:p.Cys621=
ENST00000676640.1:c.1863T>C	ENSP00000503281.1:p.Cys621=
ENST00000676803.1:c.924T>C	ENSP00000503093.1:p.Cys308=
ENST00000676835.1:c.*1078T>C	ENSP00000502911.1:n.*1078T>C
ENST00000677029.1:c.1407T>C	ENSP00000502936.1:p.Cys469=
ENST00000677099.1:c.*1573T>C	ENSP00000504553.1:n.*1573T>C
ENST00000677216.1:c.1512T>C	ENSP00000503772.1:p.Cys504=
ENST00000677221.1:n.888T>C
ENST00000677295.1:c.*1203-118T>C	ENSP00000504346.1:n.*1203-118T>C
ENST00000677444.1:c.1808T>C
ENST00000677586.1:n.1230T>C
ENST00000677626.1:c.1512T>C	ENSP00000503552.1:p.Cys504=
ENST00000677853.1:c.*871T>C	ENSP00000503488.1:n.*871T>C
ENST00000678202.1:n.1022T>C
ENST00000678264.1:c.*1240T>C	ENSP00000503157.1:n.*1240T>C
ENST00000678303.1:c.1773T>C	ENSP00000503696.1:p.Cys591=
ENST00000678366.1:c.*2112T>C	ENSP00000504353.1:n.*2112T>C
ENST00000678546.1:c.*1808T>C	ENSP00000503062.1:n.*1808T>C
ENST00000678548.1:c.*2002T>C	ENSP00000503934.1:n.*2002T>C
ENST00000678626.1:n.1699T>C
ENST00000678739.1:c.*2147-118T>C	ENSP00000503806.1:n.*2147-118T>C
ENST00000678833.1:c.*1615T>C	ENSP00000503893.1:n.*1615T>C
ENST00000679023.1:c.1701T>C	ENSP00000503718.1:p.Cys567=
ENST00000679076.1:c.1482T>C
ENST00000679111.1:c.*619T>C	ENSP00000504257.1:n.*619T>C
ENST00000679189.1:c.1512T>C	ENSP00000503356.1:p.Cys504=
ENST00000341012.11:c.1701T>C	ENSP00000343034.7:p.Cys567=
ENST00000372220.4:c.726T>C	ENSP00000361294.4:p.Cys242=
ENST00000372228.7:c.1929T>C	ENSP00000361302.3:p.Cys643=
ENST00000402686.7:c.1863T>C	ENSP00000385797.3:p.Cys621=
ENST00000404875.6:c.1512T>C	ENSP00000384531.2:p.Cys504=
ENST00000423007.5:c.1863T>C	ENSP00000404119.1:p.Cys621=
ENST00000485278.5:n.2413T>C
ENST00000494883.1:n.406T>C
NM_001077365.1:c.1863T>C	NP_001070833.1:p.Cys621=
NM_001077366.1:c.1701T>C	NP_001070834.1:p.Cys567=
NM_001136113.1:c.1863T>C	NP_001129585.1:p.Cys621=
NM_001136114.1:c.1512T>C	NP_001129586.1:p.Cys504=
NM_007171.3:c.1929T>C	NP_009102.3:p.Cys643=
XM_005272156.1:c.1929T>C	XP_005272213.1:p.Cys643=
XM_005272158.1:c.1767T>C	XP_005272215.1:p.Cys589=
XM_005272159.1:c.1578T>C	XP_005272216.1:p.Cys526=
XM_005272162.1:c.732T>C	XP_005272219.1:p.Cys244=
XM_006716932.1:c.1578T>C	XP_006716995.1:p.Cys526=
XM_011518140.1:c.1782T>C	XP_011516442.1:p.Cys594=
XM_011518141.1:c.1716T>C	XP_011516443.1:p.Cys572=
XM_011518142.1:c.1620T>C	XP_011516444.1:p.Cys540=
XM_011518143.1:c.1614T>C	XP_011516445.1:p.Cys538=
XM_011518145.1:c.1473T>C	XP_011516447.1:p.Cys491=
XM_011518147.1:c.801T>C	XP_011516449.1:p.Cys267=
XR_929703.1:n.2105T>C
NM_001353193.1:c.1929T>C	NP_001340122.1:p.Cys643=
NM_001353194.1:c.1701T>C	NP_001340123.1:p.Cys567=
NM_001353195.1:c.1512T>C	NP_001340124.1:p.Cys504=
NM_001353196.1:c.1773T>C	NP_001340125.1:p.Cys591=
NM_001353197.1:c.1767T>C	NP_001340126.1:p.Cys589=
NM_001353198.1:c.1767T>C	NP_001340127.1:p.Cys589=
NM_001353199.1:c.1578T>C	NP_001340128.1:p.Cys526=
NM_001353200.1:c.1407T>C	NP_001340129.1:p.Cys469=
NR_148391.1:n.1913T>C
NR_148392.1:n.2131T>C
NR_148393.1:n.2052T>C
NR_148394.1:n.1806T>C
NR_148395.1:n.2204T>C
NR_148396.1:n.1838T>C
NR_148397.1:n.1963T>C
NR_148398.1:n.1918T>C
NR_148399.1:n.2444T>C
NR_148400.1:n.2043T>C
XM_005272162.3:c.732T>C	XP_005272219.1:p.Cys244=
XM_006716932.2:c.1578T>C	XP_006716995.1:p.Cys526=
XM_011518140.2:c.1782T>C	XP_011516442.1:p.Cys594=
XM_011518141.2:c.1716T>C	XP_011516443.1:p.Cys572=
XM_011518142.2:c.1620T>C	XP_011516444.1:p.Cys540=
XM_011518143.2:c.1614T>C	XP_011516445.1:p.Cys538=
XM_011518145.2:c.1473T>C	XP_011516447.1:p.Cys491=
XM_017014205.2:c.732T>C	XP_016869694.1:p.Cys244=
XM_024447380.1:c.732T>C	XP_024303148.1:p.Cys244=
XM_024447381.1:c.1038T>C	XP_024303149.1:p.Cys346=
XM_024447382.1:c.732T>C	XP_024303150.1:p.Cys244=
XR_001746160.2:n.2033T>C
XR_001746162.2:n.2238T>C
XR_001746164.1:n.1955T>C
XR_001746166.2:n.2250T>C
NM_001077365.2:c.1863T>C MANE Select	NP_001070833.1:p.Cys621=
NM_001077366.2:c.1701T>C	NP_001070834.1:p.Cys567=
NM_001136113.2:c.1863T>C	NP_001129585.1:p.Cys621=
NM_001136114.2:c.1512T>C	NP_001129586.1:p.Cys504=
NM_001353193.2:c.1929T>C	NP_001340122.2:p.Cys643=
NM_001353194.2:c.1701T>C	NP_001340123.1:p.Cys567=
NM_001353195.2:c.1512T>C	NP_001340124.1:p.Cys504=
NM_001353196.2:c.1773T>C	NP_001340125.1:p.Cys591=
NM_001353197.2:c.1767T>C	NP_001340126.2:p.Cys589=
NM_001353198.2:c.1767T>C	NP_001340127.2:p.Cys589=
NM_001353199.2:c.1578T>C	NP_001340128.2:p.Cys526=
NM_001353200.2:c.1407T>C	NP_001340129.1:p.Cys469=
NM_001374689.1:c.1851T>C	NP_001361618.1:p.Cys617=
NM_001374690.1:c.1644T>C	NP_001361619.1:p.Cys548=
NM_001374691.1:c.1512T>C	NP_001361620.1:p.Cys504=
NM_001374692.1:c.1512T>C	NP_001361621.1:p.Cys504=
NM_001374693.1:c.1512T>C	NP_001361622.1:p.Cys504=
NM_001374695.1:c.1473T>C	NP_001361624.1:p.Cys491=
NM_007171.4:c.1929T>C	NP_009102.4:p.Cys643=
NR_148391.2:n.1897T>C
NR_148392.2:n.2115T>C
NR_148393.2:n.2036T>C
NR_148394.2:n.1790T>C
NR_148395.2:n.2188T>C
NR_148396.2:n.1822T>C
NR_148397.2:n.1947T>C
NR_148398.2:n.1902T>C
NR_148399.2:n.2428T>C
NR_148400.2:n.2027T>C