Canonical Allele Identifier: CA1881761413

Gene: POMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131523549G= , CM000671.2:g.131523549G=	GRCh38
NC_000009.11:g.134398936G= , CM000671.1:g.134398936G=	GRCh37
NC_000009.10:g.133388757G=	NCBI36
NG_008896.1:g.25648G=
NG_008896.2:g.25648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.*443G=	ENSP00000343034.7:n.*443G=
ENST00000404875.7:n.3161G=
ENST00000677295.2:c.*2965G=	ENSP00000504346.2:n.*2965G=
ENST00000678264.2:c.*2804G=	ENSP00000503157.2:n.*2804G=
ENST00000682070.1:n.2931G=
ENST00000682639.1:c.326G=
ENST00000682813.1:n.3018G=
ENST00000683231.1:c.471G=
ENST00000683392.1:n.5213G=
ENST00000683900.1:n.4521G=
ENST00000684062.1:n.3287G=
ENST00000684399.1:c.436G=
ENST00000684579.1:n.4467G=
ENST00000341012.12:c.*443G=	ENSP00000343034.7:n.*443G=
ENST00000372220.5:c.*443G=	ENSP00000361294.5:n.*443G=
ENST00000372228.9:c.*443G=	ENSP00000361302.3:n.*443G=
ENST00000402686.8:c.*443G= MANE Select	ENSP00000385797.4:n.*443G=
ENST00000676640.1:c.*443G=	ENSP00000503281.1:n.*443G=
ENST00000676803.1:c.*443G=	ENSP00000503093.1:n.*443G=
ENST00000676835.1:c.*1836G=	ENSP00000502911.1:n.*1836G=
ENST00000677295.1:c.*1843G=	ENSP00000504346.1:n.*1843G=
ENST00000677444.1:c.2566G=
ENST00000677626.1:c.*443G=	ENSP00000503552.1:n.*443G=
ENST00000677853.1:c.*1629G=	ENSP00000503488.1:n.*1629G=
ENST00000678546.1:c.*2566G=	ENSP00000503062.1:n.*2566G=
ENST00000678548.1:c.*2760G=	ENSP00000503934.1:n.*2760G=
ENST00000678626.1:n.2457G=
ENST00000678739.1:c.*2787G=	ENSP00000503806.1:n.*2787G=
ENST00000678833.1:c.*2373G=	ENSP00000503893.1:n.*2373G=
ENST00000679023.1:c.*267G=	ENSP00000503718.1:n.*267G=
ENST00000679076.1:c.2240G=
ENST00000679111.1:c.*1377G=	ENSP00000504257.1:n.*1377G=
ENST00000341012.11:c.*443G=	ENSP00000343034.7:n.*443G=
ENST00000372220.4:c.1484G=	ENSP00000361294.4:n.1484G=
ENST00000372228.7:c.*443G=	ENSP00000361302.3:n.*443G=
ENST00000402686.7:c.*443G=	ENSP00000385797.3:n.*443G=
ENST00000404875.6:c.*443G=	ENSP00000384531.2:n.*443G=
ENST00000423007.5:c.*443G=	ENSP00000404119.1:n.*443G=
ENST00000485278.5:n.3171G=
NM_001077365.1:c.*443G=	NP_001070833.1:n.*443G=
NM_001077366.1:c.*443G=	NP_001070834.1:n.*443G=
NM_001136113.1:c.*443G=	NP_001129585.1:n.*443G=
NM_001136114.1:c.*443G=	NP_001129586.1:n.*443G=
NM_007171.3:c.*443G=	NP_009102.3:n.*443G=
XM_005272156.1:c.*443G=	XP_005272213.1:n.*443G=
XM_005272158.1:c.*443G=	XP_005272215.1:n.*443G=
XM_005272159.1:c.*443G=	XP_005272216.1:n.*443G=
XM_005272162.1:c.*443G=	XP_005272219.1:n.*443G=
XM_006716932.1:c.*443G=	XP_006716995.1:n.*443G=
XM_011518140.1:c.*443G=	XP_011516442.1:n.*443G=
XM_011518141.1:c.*443G=	XP_011516443.1:n.*443G=
XM_011518142.1:c.*443G=	XP_011516444.1:n.*443G=
XM_011518143.1:c.*443G=	XP_011516445.1:n.*443G=
XM_011518145.1:c.*443G=	XP_011516447.1:n.*443G=
XM_011518147.1:c.*443G=	XP_011516449.1:n.*443G=
XR_929703.1:n.2687G=
NM_001353193.1:c.*443G=	NP_001340122.1:n.*443G=
NM_001353194.1:c.*443G=	NP_001340123.1:n.*443G=
NM_001353195.1:c.*443G=	NP_001340124.1:n.*443G=
NM_001353196.1:c.*443G=	NP_001340125.1:n.*443G=
NM_001353197.1:c.*443G=	NP_001340126.1:n.*443G=
NM_001353198.1:c.*443G=	NP_001340127.1:n.*443G=
NM_001353199.1:c.*443G=	NP_001340128.1:n.*443G=
NM_001353200.1:c.*443G=	NP_001340129.1:n.*443G=
NR_148391.1:n.2495G=
NR_148392.1:n.2713G=
NR_148393.1:n.2810G=
NR_148394.1:n.2564G=
NR_148395.1:n.2962G=
NR_148396.1:n.2596G=
NR_148397.1:n.2721G=
NR_148398.1:n.2676G=
NR_148399.1:n.3026G=
NR_148400.1:n.2801G=
XM_005272162.3:c.*443G=	XP_005272219.1:n.*443G=
XM_006716932.2:c.*443G=	XP_006716995.1:n.*443G=
XM_011518140.2:c.*443G=	XP_011516442.1:n.*443G=
XM_011518141.2:c.*443G=	XP_011516443.1:n.*443G=
XM_011518142.2:c.*443G=	XP_011516444.1:n.*443G=
XM_011518143.2:c.*443G=	XP_011516445.1:n.*443G=
XM_011518145.2:c.*443G=	XP_011516447.1:n.*443G=
XM_017014205.2:c.*443G=	XP_016869694.1:n.*443G=
XM_024447380.1:c.*443G=	XP_024303148.1:n.*443G=
XM_024447381.1:c.*443G=	XP_024303149.1:n.*443G=
XM_024447382.1:c.*443G=	XP_024303150.1:n.*443G=
XR_001746160.2:n.2615G=
XR_001746162.2:n.2996G=
XR_001746164.1:n.2713G=
XR_001746166.2:n.2832G=
NM_001077365.2:c.*443G= MANE Select	NP_001070833.1:n.*443G=
NM_001077366.2:c.*443G=	NP_001070834.1:n.*443G=
NM_001136113.2:c.*443G=	NP_001129585.1:n.*443G=
NM_001136114.2:c.*443G=	NP_001129586.1:n.*443G=
NM_001353193.2:c.*443G=	NP_001340122.2:n.*443G=
NM_001353194.2:c.*443G=	NP_001340123.1:n.*443G=
NM_001353195.2:c.*443G=	NP_001340124.1:n.*443G=
NM_001353196.2:c.*443G=	NP_001340125.1:n.*443G=
NM_001353197.2:c.*443G=	NP_001340126.2:n.*443G=
NM_001353198.2:c.*443G=	NP_001340127.2:n.*443G=
NM_001353199.2:c.*443G=	NP_001340128.2:n.*443G=
NM_001353200.2:c.*443G=	NP_001340129.1:n.*443G=
NM_001374689.1:c.*443G=	NP_001361618.1:n.*443G=
NM_001374690.1:c.*443G=	NP_001361619.1:n.*443G=
NM_001374691.1:c.*443G=	NP_001361620.1:n.*443G=
NM_001374692.1:c.*443G=	NP_001361621.1:n.*443G=
NM_001374693.1:c.*443G=	NP_001361622.1:n.*443G=
NM_001374695.1:c.*443G=	NP_001361624.1:n.*443G=
NM_007171.4:c.*443G=	NP_009102.4:n.*443G=
NR_148391.2:n.2479G=
NR_148392.2:n.2697G=
NR_148393.2:n.2794G=
NR_148394.2:n.2548G=
NR_148395.2:n.2946G=
NR_148396.2:n.2580G=
NR_148397.2:n.2705G=
NR_148398.2:n.2660G=
NR_148399.2:n.3010G=
NR_148400.2:n.2785G=