Canonical Allele Identifier: CA1484811059
Gene: EGF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109980906C= , CM000666.2:g.109980906C= GRCh38
NC_000004.11:g.110902062C= , CM000666.1:g.110902062C= GRCh37
NC_000004.10:g.111121511C= NCBI36
NG_011441.1:g.73023C=
NG_011441.2:g.73023C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265171.10:c.2302C= MANE Select ENSP00000265171.5:p.Arg768=
ENST00000652245.1:c.2176C= ENSP00000498337.1:p.Arg726=
ENST00000265171.9:c.2302C= ENSP00000265171.5:p.Arg768=
ENST00000503392.1:c.2302C= ENSP00000421384.1:p.Arg768=
ENST00000509793.5:c.2176C= ENSP00000424316.1:p.Arg726=
ENST00000509996.1:n.230C=
ENST00000511228.5:n.266C=
NM_001178130.1:c.2302C= NP_001171601.1:p.Arg768=
NM_001178131.1:c.2176C= NP_001171602.1:p.Arg726=
NM_001963.4:c.2302C= NP_001954.2:p.Arg768=
XM_005262796.2:c.2302C= XP_005262853.1:p.Arg768=
XM_005262797.2:c.2176C= XP_005262854.1:p.Arg726=
XM_005262798.2:c.2302C= XP_005262855.1:p.Arg768=
XM_005262800.2:c.2302C= XP_005262857.1:p.Arg768=
XM_005262801.2:c.2302C= XP_005262858.1:p.Arg768=
XM_006714124.2:c.2302C= XP_006714187.1:p.Arg768=
XM_011531707.1:c.2191C= XP_011530009.1:p.Arg731=
XM_011531708.1:c.2302C= XP_011530010.1:p.Arg768=
XR_427532.2:n.2755C=
XR_938699.1:n.2755C=
NM_001178130.2:c.2302C= NP_001171601.1:p.Arg768=
NM_001178131.2:c.2176C= NP_001171602.1:p.Arg726=
NM_001357021.1:c.2176C= NP_001343950.1:p.Arg726=
NM_001963.5:c.2302C= NP_001954.2:p.Arg768=
XM_017007845.1:c.2326C= XP_016863334.1:p.Arg776=
XM_017007846.1:c.2326C= XP_016863335.1:p.Arg776=
XM_017007847.1:c.2326C= XP_016863336.1:p.Arg776=
XM_017007848.1:c.2200C= XP_016863337.1:p.Arg734=
XM_017007849.1:c.2326C= XP_016863338.1:p.Arg776=
XM_017007850.1:c.2326C= XP_016863339.1:p.Arg776=
XM_017007851.1:c.2326C= XP_016863340.1:p.Arg776=
XM_017007853.1:c.2326C= XP_016863342.1:p.Arg776=
XR_001741156.1:n.2779C=
XR_001741157.1:n.2779C=
NM_001178130.3:c.2302C= NP_001171601.1:p.Arg768=
NM_001178131.3:c.2176C= NP_001171602.1:p.Arg726=
NM_001357021.2:c.2176C= NP_001343950.1:p.Arg726=
NM_001963.6:c.2302C= MANE Select NP_001954.2:p.Arg768=