Canonical Allele Identifier: CA16621851
Gene: SYNE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425399
ClinVar RCV Id: RCV000487909
dbSNP Id: rs1064797332

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152395671del , CM000668.2:g.152395671del GRCh38
NC_000006.11:g.152716806del , CM000668.1:g.152716806del GRCh37
NC_000006.10:g.152758499del NCBI36
NG_012855.1:g.246729del
NG_012855.2:g.246729del

Transcript Alleles

HGVS Amino-acid change
ENST00000367255.10:c.7557del MANE Select ENSP00000356224.5:p.Phe2520LeufsTer8
ENST00000423061.6:c.7578del ENSP00000396024.1:p.Phe2527LeufsTer8
ENST00000341594.9:c.7623del ENSP00000341887.6:p.Phe2542LeufsTer8
ENST00000367255.9:c.7557del ENSP00000356224.5:p.Phe2520LeufsTer8
ENST00000423061.5:c.7578del ENSP00000396024.1:p.Phe2527LeufsTer8
ENST00000461872.6:n.7775del
NM_033071.3:c.7578del NP_149062.1:p.Phe2527LeufsTer8
NM_182961.3:c.7557del NP_892006.3:p.Phe2520LeufsTer8
XM_006715407.1:c.7578del XP_006715470.1:p.Phe2527LeufsTer8
XM_006715408.1:c.7578del XP_006715471.1:p.Phe2527LeufsTer8
XM_006715409.1:c.7557del XP_006715472.1:p.Phe2520LeufsTer8
XM_006715410.1:c.7578del XP_006715473.1:p.Phe2527LeufsTer8
XM_006715411.1:c.7527del XP_006715474.1:p.Phe2510LeufsTer8
XM_006715412.1:c.7578del XP_006715475.1:p.Phe2527LeufsTer8
XM_006715413.1:c.7578del XP_006715476.1:p.Phe2527LeufsTer8
XM_006715414.1:c.7506del XP_006715477.1:p.Phe2503LeufsTer8
XM_006715415.1:c.7578del XP_006715478.1:p.Phe2527LeufsTer8
XM_006715416.1:c.7578del XP_006715479.1:p.Phe2527LeufsTer8
XM_006715417.1:c.7578del XP_006715480.1:p.Phe2527LeufsTer8
XM_006715420.1:c.7578del XP_006715483.1:p.Phe2527LeufsTer8
XM_006715421.1:c.7578del XP_006715484.1:p.Phe2527LeufsTer8
XM_006715422.1:c.7419del XP_006715485.1:p.Phe2474LeufsTer8
XM_006715423.1:c.7578del XP_006715486.1:p.Phe2527LeufsTer8
XM_006715424.1:c.7578del XP_006715487.1:p.Phe2527LeufsTer8
XM_006715425.1:c.7578del XP_006715488.1:p.Phe2527LeufsTer8
XM_011535641.1:c.7578del XP_011533943.1:p.Phe2527LeufsTer8
XM_011535642.1:c.7578del XP_011533944.1:p.Phe2527LeufsTer8
XM_011535643.1:c.7413del XP_011533945.1:p.Phe2472LeufsTer8
XM_011535644.1:c.5853del XP_011533946.1:p.Phe1952LeufsTer8
XM_011535645.1:c.5346del XP_011533947.1:p.Phe1783LeufsTer8
XM_011535646.1:c.7578del XP_011533948.1:p.Phe2527LeufsTer8
XM_011535647.1:c.813del XP_011533949.1:p.Phe272LeufsTer8
XM_006715408.2:c.7578del XP_006715471.1:p.Phe2527LeufsTer8
XM_006715410.2:c.7578del XP_006715473.1:p.Phe2527LeufsTer8
XM_006715412.2:c.7578del XP_006715475.1:p.Phe2527LeufsTer8
XM_006715413.2:c.7578del XP_006715476.1:p.Phe2527LeufsTer8
XM_006715415.2:c.7578del XP_006715478.1:p.Phe2527LeufsTer8
XM_006715416.2:c.7578del XP_006715479.1:p.Phe2527LeufsTer8
XM_006715417.2:c.7578del XP_006715480.1:p.Phe2527LeufsTer8
XM_006715420.2:c.7578del XP_006715483.1:p.Phe2527LeufsTer8
XM_006715421.2:c.7578del XP_006715484.1:p.Phe2527LeufsTer8
XM_006715423.2:c.7578del XP_006715486.1:p.Phe2527LeufsTer8
XM_006715424.2:c.7578del XP_006715487.1:p.Phe2527LeufsTer8
XM_006715425.2:c.7578del XP_006715488.1:p.Phe2527LeufsTer8
XM_011535641.2:c.7578del XP_011533943.1:p.Phe2527LeufsTer8
XM_011535642.2:c.7578del XP_011533944.1:p.Phe2527LeufsTer8
XM_011535645.2:c.5346del XP_011533947.1:p.Phe1783LeufsTer8
XM_017010608.1:c.7578del XP_016866097.1:p.Phe2527LeufsTer8
XM_017010609.1:c.7578del XP_016866098.1:p.Phe2527LeufsTer8
XM_017010610.1:c.7557del XP_016866099.1:p.Phe2520LeufsTer8
XM_017010611.2:c.7551del XP_016866100.1:p.Phe2518LeufsTer8
XM_017010612.1:c.7500del XP_016866101.1:p.Phe2501LeufsTer8
XM_017010613.1:c.7578del XP_016866102.1:p.Phe2527LeufsTer8
XM_017010614.1:c.7578del XP_016866103.1:p.Phe2527LeufsTer8
XM_017010615.1:c.7578del XP_016866104.1:p.Phe2527LeufsTer8
XM_017010616.1:c.7578del XP_016866105.1:p.Phe2527LeufsTer8
XM_017010617.1:c.7578del XP_016866106.1:p.Phe2527LeufsTer8
XM_017010618.1:c.7578del XP_016866107.1:p.Phe2527LeufsTer8
XM_017010619.1:c.5853del XP_016866108.1:p.Phe1952LeufsTer8
XR_001743287.1:n.8061del
NM_182961.4:c.7557del MANE Select NP_892006.3:p.Phe2520LeufsTer8
NM_033071.5:c.7578del NP_149062.2:p.Phe2527LeufsTer8