Canonical Allele Identifier: CA2692223859
Gene: POMT1 HGNC NCBI

Linked Data

gnomAD v4: 9-131523547-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523547C>A , CM000671.2:g.131523547C>A GRCh38
NC_000009.11:g.134398934C>A , CM000671.1:g.134398934C>A GRCh37
NC_000009.10:g.133388755C>A NCBI36
NG_008896.1:g.25646C>A
NG_008896.2:g.25646C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.*441C>A ENSP00000343034.7:n.*441C>A
ENST00000404875.7:n.3159C>A
ENST00000677295.2:c.*2963C>A ENSP00000504346.2:n.*2963C>A
ENST00000678264.2:c.*2802C>A ENSP00000503157.2:n.*2802C>A
ENST00000682070.1:n.2929C>A
ENST00000682639.1:c.324C>A
ENST00000682813.1:n.3016C>A
ENST00000683231.1:c.469C>A
ENST00000683392.1:n.5211C>A
ENST00000683900.1:n.4519C>A
ENST00000684062.1:n.3285C>A
ENST00000684399.1:c.434C>A
ENST00000684579.1:n.4465C>A
ENST00000341012.12:c.*441C>A ENSP00000343034.7:n.*441C>A
ENST00000372220.5:c.*441C>A ENSP00000361294.5:n.*441C>A
ENST00000372228.9:c.*441C>A ENSP00000361302.3:n.*441C>A
ENST00000402686.8:c.*441C>A MANE Select ENSP00000385797.4:n.*441C>A
ENST00000676640.1:c.*441C>A ENSP00000503281.1:n.*441C>A
ENST00000676803.1:c.*441C>A ENSP00000503093.1:n.*441C>A
ENST00000676835.1:c.*1834C>A ENSP00000502911.1:n.*1834C>A
ENST00000677295.1:c.*1841C>A ENSP00000504346.1:n.*1841C>A
ENST00000677444.1:c.2564C>A
ENST00000677626.1:c.*441C>A ENSP00000503552.1:n.*441C>A
ENST00000677853.1:c.*1627C>A ENSP00000503488.1:n.*1627C>A
ENST00000678546.1:c.*2564C>A ENSP00000503062.1:n.*2564C>A
ENST00000678548.1:c.*2758C>A ENSP00000503934.1:n.*2758C>A
ENST00000678626.1:n.2455C>A
ENST00000678739.1:c.*2785C>A ENSP00000503806.1:n.*2785C>A
ENST00000678833.1:c.*2371C>A ENSP00000503893.1:n.*2371C>A
ENST00000679023.1:c.*265C>A ENSP00000503718.1:n.*265C>A
ENST00000679076.1:c.2238C>A
ENST00000679111.1:c.*1375C>A ENSP00000504257.1:n.*1375C>A
ENST00000341012.11:c.*441C>A ENSP00000343034.7:n.*441C>A
ENST00000372220.4:c.1482C>A ENSP00000361294.4:n.1482C>A
ENST00000372228.7:c.*441C>A ENSP00000361302.3:n.*441C>A
ENST00000402686.7:c.*441C>A ENSP00000385797.3:n.*441C>A
ENST00000404875.6:c.*441C>A ENSP00000384531.2:n.*441C>A
ENST00000423007.5:c.*441C>A ENSP00000404119.1:n.*441C>A
ENST00000485278.5:n.3169C>A
NM_001077365.1:c.*441C>A NP_001070833.1:n.*441C>A
NM_001077366.1:c.*441C>A NP_001070834.1:n.*441C>A
NM_001136113.1:c.*441C>A NP_001129585.1:n.*441C>A
NM_001136114.1:c.*441C>A NP_001129586.1:n.*441C>A
NM_007171.3:c.*441C>A NP_009102.3:n.*441C>A
XM_005272156.1:c.*441C>A XP_005272213.1:n.*441C>A
XM_005272158.1:c.*441C>A XP_005272215.1:n.*441C>A
XM_005272159.1:c.*441C>A XP_005272216.1:n.*441C>A
XM_005272162.1:c.*441C>A XP_005272219.1:n.*441C>A
XM_006716932.1:c.*441C>A XP_006716995.1:n.*441C>A
XM_011518140.1:c.*441C>A XP_011516442.1:n.*441C>A
XM_011518141.1:c.*441C>A XP_011516443.1:n.*441C>A
XM_011518142.1:c.*441C>A XP_011516444.1:n.*441C>A
XM_011518143.1:c.*441C>A XP_011516445.1:n.*441C>A
XM_011518145.1:c.*441C>A XP_011516447.1:n.*441C>A
XM_011518147.1:c.*441C>A XP_011516449.1:n.*441C>A
XR_929703.1:n.2685C>A
NM_001353193.1:c.*441C>A NP_001340122.1:n.*441C>A
NM_001353194.1:c.*441C>A NP_001340123.1:n.*441C>A
NM_001353195.1:c.*441C>A NP_001340124.1:n.*441C>A
NM_001353196.1:c.*441C>A NP_001340125.1:n.*441C>A
NM_001353197.1:c.*441C>A NP_001340126.1:n.*441C>A
NM_001353198.1:c.*441C>A NP_001340127.1:n.*441C>A
NM_001353199.1:c.*441C>A NP_001340128.1:n.*441C>A
NM_001353200.1:c.*441C>A NP_001340129.1:n.*441C>A
NR_148391.1:n.2493C>A
NR_148392.1:n.2711C>A
NR_148393.1:n.2808C>A
NR_148394.1:n.2562C>A
NR_148395.1:n.2960C>A
NR_148396.1:n.2594C>A
NR_148397.1:n.2719C>A
NR_148398.1:n.2674C>A
NR_148399.1:n.3024C>A
NR_148400.1:n.2799C>A
XM_005272162.3:c.*441C>A XP_005272219.1:n.*441C>A
XM_006716932.2:c.*441C>A XP_006716995.1:n.*441C>A
XM_011518140.2:c.*441C>A XP_011516442.1:n.*441C>A
XM_011518141.2:c.*441C>A XP_011516443.1:n.*441C>A
XM_011518142.2:c.*441C>A XP_011516444.1:n.*441C>A
XM_011518143.2:c.*441C>A XP_011516445.1:n.*441C>A
XM_011518145.2:c.*441C>A XP_011516447.1:n.*441C>A
XM_017014205.2:c.*441C>A XP_016869694.1:n.*441C>A
XM_024447380.1:c.*441C>A XP_024303148.1:n.*441C>A
XM_024447381.1:c.*441C>A XP_024303149.1:n.*441C>A
XM_024447382.1:c.*441C>A XP_024303150.1:n.*441C>A
XR_001746160.2:n.2613C>A
XR_001746162.2:n.2994C>A
XR_001746164.1:n.2711C>A
XR_001746166.2:n.2830C>A
NM_001077365.2:c.*441C>A MANE Select NP_001070833.1:n.*441C>A
NM_001077366.2:c.*441C>A NP_001070834.1:n.*441C>A
NM_001136113.2:c.*441C>A NP_001129585.1:n.*441C>A
NM_001136114.2:c.*441C>A NP_001129586.1:n.*441C>A
NM_001353193.2:c.*441C>A NP_001340122.2:n.*441C>A
NM_001353194.2:c.*441C>A NP_001340123.1:n.*441C>A
NM_001353195.2:c.*441C>A NP_001340124.1:n.*441C>A
NM_001353196.2:c.*441C>A NP_001340125.1:n.*441C>A
NM_001353197.2:c.*441C>A NP_001340126.2:n.*441C>A
NM_001353198.2:c.*441C>A NP_001340127.2:n.*441C>A
NM_001353199.2:c.*441C>A NP_001340128.2:n.*441C>A
NM_001353200.2:c.*441C>A NP_001340129.1:n.*441C>A
NM_001374689.1:c.*441C>A NP_001361618.1:n.*441C>A
NM_001374690.1:c.*441C>A NP_001361619.1:n.*441C>A
NM_001374691.1:c.*441C>A NP_001361620.1:n.*441C>A
NM_001374692.1:c.*441C>A NP_001361621.1:n.*441C>A
NM_001374693.1:c.*441C>A NP_001361622.1:n.*441C>A
NM_001374695.1:c.*441C>A NP_001361624.1:n.*441C>A
NM_007171.4:c.*441C>A NP_009102.4:n.*441C>A
NR_148391.2:n.2477C>A
NR_148392.2:n.2695C>A
NR_148393.2:n.2792C>A
NR_148394.2:n.2546C>A
NR_148395.2:n.2944C>A
NR_148396.2:n.2578C>A
NR_148397.2:n.2703C>A
NR_148398.2:n.2658C>A
NR_148399.2:n.3008C>A
NR_148400.2:n.2783C>A
Search 100 bp 5'
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