Canonical Allele Identifier: CA2671756668
Gene: EGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110011715_110011723del , CM000666.2:g.110011715_110011723del GRCh38
NC_000004.11:g.110932871_110932879del , CM000666.1:g.110932871_110932879del GRCh37
NC_000004.10:g.111152320_111152328del NCBI36
NG_011441.1:g.103832_103840del
NG_011441.2:g.103832_103840del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265171.10:c.*260_*268del MANE Select ENSP00000265171.5:n.*260_*268del
ENST00000652245.1:c.*403_*411del ENSP00000498337.1:n.*403_*411del
ENST00000265171.9:c.*260_*268del ENSP00000265171.5:n.*260_*268del
ENST00000509793.5:c.*260_*268del ENSP00000424316.1:n.*260_*268del
ENST00000540840.1:n.229+407_230-403del
NM_001178130.1:c.*260_*268del NP_001171601.1:n.*260_*268del
NM_001178131.1:c.*260_*268del NP_001171602.1:n.*260_*268del
NM_001963.4:c.*260_*268del NP_001954.2:n.*260_*268del
XM_005262796.2:c.*260_*268del XP_005262853.1:n.*260_*268del
XM_005262797.2:c.*260_*268del XP_005262854.1:n.*260_*268del
XM_005262798.2:c.*260_*268del XP_005262855.1:n.*260_*268del
XM_005262800.2:c.*403_*411del XP_005262857.1:n.*403_*411del
XM_005262801.2:c.*260_*268del XP_005262858.1:n.*260_*268del
XM_006714124.2:c.*403_*411del XP_006714187.1:n.*403_*411del
XM_011531707.1:c.*260_*268del XP_011530009.1:n.*260_*268del
NM_001178130.2:c.*260_*268del NP_001171601.1:n.*260_*268del
NM_001178131.2:c.*260_*268del NP_001171602.1:n.*260_*268del
NM_001357021.1:c.*403_*411del NP_001343950.1:n.*403_*411del
NM_001963.5:c.*260_*268del NP_001954.2:n.*260_*268del
XM_017007845.1:c.*260_*268del XP_016863334.1:n.*260_*268del
XM_017007846.1:c.*260_*268del XP_016863335.1:n.*260_*268del
XM_017007847.1:c.*260_*268del XP_016863336.1:n.*260_*268del
XM_017007848.1:c.*260_*268del XP_016863337.1:n.*260_*268del
XM_017007849.1:c.*260_*268del XP_016863338.1:n.*260_*268del
XM_017007850.1:c.*403_*411del XP_016863339.1:n.*403_*411del
XM_017007851.1:c.*403_*411del XP_016863340.1:n.*403_*411del
NM_001178130.3:c.*260_*268del NP_001171601.1:n.*260_*268del
NM_001178131.3:c.*260_*268del NP_001171602.1:n.*260_*268del
NM_001357021.2:c.*403_*411del NP_001343950.1:n.*403_*411del
NM_001963.6:c.*260_*268del MANE Select NP_001954.2:n.*260_*268del