Canonical Allele Identifier: CA2692223798

Gene: POMT1

Linked Data

• gnomAD v4: 9-131523535-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131523535C>G , CM000671.2:g.131523535C>G	GRCh38
NC_000009.11:g.134398922C>G , CM000671.1:g.134398922C>G	GRCh37
NC_000009.10:g.133388743C>G	NCBI36
NG_008896.1:g.25634C>G
NG_008896.2:g.25634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.*429C>G	ENSP00000343034.7:n.*429C>G
ENST00000404875.7:n.3147C>G
ENST00000677295.2:c.*2951C>G	ENSP00000504346.2:n.*2951C>G
ENST00000678264.2:c.*2790C>G	ENSP00000503157.2:n.*2790C>G
ENST00000682070.1:n.2917C>G
ENST00000682639.1:c.312C>G
ENST00000682813.1:n.3004C>G
ENST00000683231.1:c.457C>G
ENST00000683392.1:n.5199C>G
ENST00000683900.1:n.4507C>G
ENST00000684062.1:n.3273C>G
ENST00000684399.1:c.422C>G
ENST00000684579.1:n.4453C>G
ENST00000341012.12:c.*429C>G	ENSP00000343034.7:n.*429C>G
ENST00000372220.5:c.*429C>G	ENSP00000361294.5:n.*429C>G
ENST00000372228.9:c.*429C>G	ENSP00000361302.3:n.*429C>G
ENST00000402686.8:c.*429C>G MANE Select	ENSP00000385797.4:n.*429C>G
ENST00000676640.1:c.*429C>G	ENSP00000503281.1:n.*429C>G
ENST00000676803.1:c.*429C>G	ENSP00000503093.1:n.*429C>G
ENST00000676835.1:c.*1822C>G	ENSP00000502911.1:n.*1822C>G
ENST00000677295.1:c.*1829C>G	ENSP00000504346.1:n.*1829C>G
ENST00000677444.1:c.2552C>G
ENST00000677626.1:c.*429C>G	ENSP00000503552.1:n.*429C>G
ENST00000677853.1:c.*1615C>G	ENSP00000503488.1:n.*1615C>G
ENST00000678546.1:c.*2552C>G	ENSP00000503062.1:n.*2552C>G
ENST00000678548.1:c.*2746C>G	ENSP00000503934.1:n.*2746C>G
ENST00000678626.1:n.2443C>G
ENST00000678739.1:c.*2773C>G	ENSP00000503806.1:n.*2773C>G
ENST00000678833.1:c.*2359C>G	ENSP00000503893.1:n.*2359C>G
ENST00000679023.1:c.*253C>G	ENSP00000503718.1:n.*253C>G
ENST00000679076.1:c.2226C>G
ENST00000679111.1:c.*1363C>G	ENSP00000504257.1:n.*1363C>G
ENST00000341012.11:c.*429C>G	ENSP00000343034.7:n.*429C>G
ENST00000372220.4:c.1470C>G	ENSP00000361294.4:n.1470C>G
ENST00000372228.7:c.*429C>G	ENSP00000361302.3:n.*429C>G
ENST00000402686.7:c.*429C>G	ENSP00000385797.3:n.*429C>G
ENST00000404875.6:c.*429C>G	ENSP00000384531.2:n.*429C>G
ENST00000423007.5:c.*429C>G	ENSP00000404119.1:n.*429C>G
ENST00000485278.5:n.3157C>G
NM_001077365.1:c.*429C>G	NP_001070833.1:n.*429C>G
NM_001077366.1:c.*429C>G	NP_001070834.1:n.*429C>G
NM_001136113.1:c.*429C>G	NP_001129585.1:n.*429C>G
NM_001136114.1:c.*429C>G	NP_001129586.1:n.*429C>G
NM_007171.3:c.*429C>G	NP_009102.3:n.*429C>G
XM_005272156.1:c.*429C>G	XP_005272213.1:n.*429C>G
XM_005272158.1:c.*429C>G	XP_005272215.1:n.*429C>G
XM_005272159.1:c.*429C>G	XP_005272216.1:n.*429C>G
XM_005272162.1:c.*429C>G	XP_005272219.1:n.*429C>G
XM_006716932.1:c.*429C>G	XP_006716995.1:n.*429C>G
XM_011518140.1:c.*429C>G	XP_011516442.1:n.*429C>G
XM_011518141.1:c.*429C>G	XP_011516443.1:n.*429C>G
XM_011518142.1:c.*429C>G	XP_011516444.1:n.*429C>G
XM_011518143.1:c.*429C>G	XP_011516445.1:n.*429C>G
XM_011518145.1:c.*429C>G	XP_011516447.1:n.*429C>G
XM_011518147.1:c.*429C>G	XP_011516449.1:n.*429C>G
XR_929703.1:n.2673C>G
NM_001353193.1:c.*429C>G	NP_001340122.1:n.*429C>G
NM_001353194.1:c.*429C>G	NP_001340123.1:n.*429C>G
NM_001353195.1:c.*429C>G	NP_001340124.1:n.*429C>G
NM_001353196.1:c.*429C>G	NP_001340125.1:n.*429C>G
NM_001353197.1:c.*429C>G	NP_001340126.1:n.*429C>G
NM_001353198.1:c.*429C>G	NP_001340127.1:n.*429C>G
NM_001353199.1:c.*429C>G	NP_001340128.1:n.*429C>G
NM_001353200.1:c.*429C>G	NP_001340129.1:n.*429C>G
NR_148391.1:n.2481C>G
NR_148392.1:n.2699C>G
NR_148393.1:n.2796C>G
NR_148394.1:n.2550C>G
NR_148395.1:n.2948C>G
NR_148396.1:n.2582C>G
NR_148397.1:n.2707C>G
NR_148398.1:n.2662C>G
NR_148399.1:n.3012C>G
NR_148400.1:n.2787C>G
XM_005272162.3:c.*429C>G	XP_005272219.1:n.*429C>G
XM_006716932.2:c.*429C>G	XP_006716995.1:n.*429C>G
XM_011518140.2:c.*429C>G	XP_011516442.1:n.*429C>G
XM_011518141.2:c.*429C>G	XP_011516443.1:n.*429C>G
XM_011518142.2:c.*429C>G	XP_011516444.1:n.*429C>G
XM_011518143.2:c.*429C>G	XP_011516445.1:n.*429C>G
XM_011518145.2:c.*429C>G	XP_011516447.1:n.*429C>G
XM_017014205.2:c.*429C>G	XP_016869694.1:n.*429C>G
XM_024447380.1:c.*429C>G	XP_024303148.1:n.*429C>G
XM_024447381.1:c.*429C>G	XP_024303149.1:n.*429C>G
XM_024447382.1:c.*429C>G	XP_024303150.1:n.*429C>G
XR_001746160.2:n.2601C>G
XR_001746162.2:n.2982C>G
XR_001746164.1:n.2699C>G
XR_001746166.2:n.2818C>G
NM_001077365.2:c.*429C>G MANE Select	NP_001070833.1:n.*429C>G
NM_001077366.2:c.*429C>G	NP_001070834.1:n.*429C>G
NM_001136113.2:c.*429C>G	NP_001129585.1:n.*429C>G
NM_001136114.2:c.*429C>G	NP_001129586.1:n.*429C>G
NM_001353193.2:c.*429C>G	NP_001340122.2:n.*429C>G
NM_001353194.2:c.*429C>G	NP_001340123.1:n.*429C>G
NM_001353195.2:c.*429C>G	NP_001340124.1:n.*429C>G
NM_001353196.2:c.*429C>G	NP_001340125.1:n.*429C>G
NM_001353197.2:c.*429C>G	NP_001340126.2:n.*429C>G
NM_001353198.2:c.*429C>G	NP_001340127.2:n.*429C>G
NM_001353199.2:c.*429C>G	NP_001340128.2:n.*429C>G
NM_001353200.2:c.*429C>G	NP_001340129.1:n.*429C>G
NM_001374689.1:c.*429C>G	NP_001361618.1:n.*429C>G
NM_001374690.1:c.*429C>G	NP_001361619.1:n.*429C>G
NM_001374691.1:c.*429C>G	NP_001361620.1:n.*429C>G
NM_001374692.1:c.*429C>G	NP_001361621.1:n.*429C>G
NM_001374693.1:c.*429C>G	NP_001361622.1:n.*429C>G
NM_001374695.1:c.*429C>G	NP_001361624.1:n.*429C>G
NM_007171.4:c.*429C>G	NP_009102.4:n.*429C>G
NR_148391.2:n.2465C>G
NR_148392.2:n.2683C>G
NR_148393.2:n.2780C>G
NR_148394.2:n.2534C>G
NR_148395.2:n.2932C>G
NR_148396.2:n.2566C>G
NR_148397.2:n.2691C>G
NR_148398.2:n.2646C>G
NR_148399.2:n.2996C>G
NR_148400.2:n.2771C>G