Canonical Allele Identifier: CA645294063
Gene: EBF3 HGNC NCBI

Linked Data

dbSNP Id: rs1085307482

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.129963372_129963373del , CM000672.2:g.129963372_129963373del GRCh38
NC_000010.10:g.131761636_131761637del , CM000672.1:g.131761636_131761637del GRCh37
NC_000010.9:g.131651626_131651627del NCBI36
NG_030038.1:g.5458_5459del

Transcript Alleles

HGVS Amino-acid change
ENST00000682649.1:n.238_239del
ENST00000355311.10:c.288_289del ENSP00000347463.4:p.Lys97ArgfsTer14
ENST00000368648.8:c.288_289del ENSP00000357637.3:p.Lys97ArgfsTer14
ENST00000440978.2:c.288_289del MANE Select ENSP00000387543.2:p.Lys97ArgfsTer14
ENST00000355311.9:c.288_289del ENSP00000347463.4:p.Lys97ArgfsTer14
ENST00000368648.7:c.288_289del ENSP00000357637.3:p.Lys97ArgfsTer14
NM_001005463.2:c.288_289del NP_001005463.1:p.Lys97ArgfsTer14
XM_005252667.2:c.288_289del XP_005252724.1:p.Lys97ArgfsTer14
XM_005252668.2:c.288_289del XP_005252725.1:p.Lys97ArgfsTer14
XM_005252669.2:c.288_289del XP_005252726.1:p.Lys97ArgfsTer14
XM_006717739.2:c.288_289del XP_006717802.1:p.Lys97ArgfsTer14
XM_006717740.2:c.288_289del XP_006717803.1:p.Lys97ArgfsTer14
XM_006717741.2:c.288_289del XP_006717804.1:p.Lys97ArgfsTer14
XM_006717742.2:c.288_289del XP_006717805.1:p.Lys97ArgfsTer14
XM_006717743.2:c.288_289del XP_006717806.1:p.Lys97ArgfsTer14
XM_006717744.2:c.288_289del XP_006717807.1:p.Lys97ArgfsTer14
XM_011539574.1:c.288_289del XP_011537876.1:p.Lys97ArgfsTer14
XM_011539576.1:c.288_289del XP_011537878.1:p.Lys97ArgfsTer14
XM_005252667.3:c.288_289del XP_005252724.1:p.Lys97ArgfsTer14
XM_005252668.3:c.288_289del XP_005252725.1:p.Lys97ArgfsTer14
XM_005252669.3:c.288_289del XP_005252726.1:p.Lys97ArgfsTer14
XM_006717739.3:c.288_289del XP_006717802.1:p.Lys97ArgfsTer14
XM_006717740.3:c.288_289del XP_006717803.1:p.Lys97ArgfsTer14
XM_006717741.3:c.288_289del XP_006717804.1:p.Lys97ArgfsTer14
XM_006717742.3:c.288_289del XP_006717805.1:p.Lys97ArgfsTer14
XM_006717743.3:c.288_289del XP_006717806.1:p.Lys97ArgfsTer14
XM_006717744.3:c.288_289del XP_006717807.1:p.Lys97ArgfsTer14
XM_011539574.2:c.288_289del XP_011537876.1:p.Lys97ArgfsTer14
XM_017016027.1:c.288_289del XP_016871516.1:p.Lys97ArgfsTer14
XR_001747076.1:n.794_795del
NM_001005463.3:c.288_289del NP_001005463.1:p.Lys97ArgfsTer14
NM_001375379.1:c.288_289del NP_001362308.1:p.Lys97ArgfsTer14
NM_001375380.1:c.288_289del MANE Select NP_001362309.1:p.Lys97ArgfsTer14
NM_001375389.1:c.288_289del NP_001362318.1:p.Lys97ArgfsTer14
NM_001375390.1:c.288_289del NP_001362319.1:p.Lys97ArgfsTer14
NM_001375391.1:c.288_289del NP_001362320.1:p.Lys97ArgfsTer14
NM_001375392.1:c.288_289del NP_001362321.1:p.Lys97ArgfsTer14