Canonical Allele Identifier: CA2671752641
Gene: EGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109945276del , CM000666.2:g.109945276del GRCh38
NC_000004.11:g.110866432del , CM000666.1:g.110866432del GRCh37
NC_000004.10:g.111085881del NCBI36
NG_011441.1:g.37393del
NG_011441.2:g.37393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265171.10:c.940+1del
ENST00000652245.1:c.940+1del
ENST00000265171.9:c.940+1del
ENST00000503392.1:c.940+1del
ENST00000509793.5:c.940+1del
NM_001178130.1:c.940+1del
NM_001178131.1:c.940+1del
NM_001963.4:c.940+1del
XM_005262796.2:c.940+1del
XM_005262797.2:c.940+1del
XM_005262798.2:c.940+1del
XM_005262800.2:c.940+1del
XM_005262801.2:c.940+1del
XM_005262802.2:c.940+1del
XM_006714124.2:c.940+1del
XM_011531707.1:c.829+1del
XM_011531708.1:c.940+1del
XM_011531709.1:c.940+1del
XR_427532.2:n.1393+1del
XR_938699.1:n.1393+1del
NM_001178130.2:c.940+1del
NM_001178131.2:c.940+1del
NM_001357021.1:c.940+1del
NM_001963.5:c.940+1del
XM_017007845.1:c.964+1del
XM_017007846.1:c.964+1del
XM_017007847.1:c.964+1del
XM_017007848.1:c.964+1del
XM_017007849.1:c.964+1del
XM_017007850.1:c.964+1del
XM_017007851.1:c.964+1del
XM_017007853.1:c.964+1del
XM_017007854.1:c.964+1del
XM_017007855.1:c.964+1del
XR_001741156.1:n.1417+1del
XR_001741157.1:n.1417+1del
NM_001178130.3:c.940+1del
NM_001178131.3:c.940+1del
NM_001357021.2:c.940+1del
NM_001963.6:c.940+1del