Canonical Allele Identifier: CA3043517
Gene: EGF HGNC NCBI

Linked Data

ClinVar Variation Id: 347230
dbSNP Id: rs4698756

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109945286G>A , CM000666.2:g.109945286G>A GRCh38
NC_000004.11:g.110866442G>A , CM000666.1:g.110866442G>A GRCh37
NC_000004.10:g.111085891G>A NCBI36
NG_011441.1:g.37403G>A
NG_011441.2:g.37403G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265171.10:c.940+11G>A MANE Select ENSP00000265171.5:p.=
ENST00000652245.1:c.940+11G>A ENSP00000498337.1:p.=
ENST00000265171.9:c.940+11G>A ENSP00000265171.5:p.=
ENST00000503392.1:c.940+11G>A ENSP00000421384.1:p.=
ENST00000509793.5:c.940+11G>A ENSP00000424316.1:p.=
NM_001178130.1:c.940+11G>A NP_001171601.1:p.=
NM_001178131.1:c.940+11G>A NP_001171602.1:p.=
NM_001963.4:c.940+11G>A NP_001954.2:p.=
XM_005262796.2:c.940+11G>A XP_005262853.1:p.=
XM_005262797.2:c.940+11G>A XP_005262854.1:p.=
XM_005262798.2:c.940+11G>A XP_005262855.1:p.=
XM_005262800.2:c.940+11G>A XP_005262857.1:p.=
XM_005262801.2:c.940+11G>A XP_005262858.1:p.=
XM_005262802.2:c.940+11G>A XP_005262859.1:p.=
XM_006714124.2:c.940+11G>A XP_006714187.1:p.=
XM_011531707.1:c.829+11G>A XP_011530009.1:p.=
XM_011531708.1:c.940+11G>A XP_011530010.1:p.=
XM_011531709.1:c.940+11G>A XP_011530011.1:p.=
XR_427532.2:n.1393+11G>A
XR_938699.1:n.1393+11G>A
NM_001178130.2:c.940+11G>A NP_001171601.1:p.=
NM_001178131.2:c.940+11G>A NP_001171602.1:p.=
NM_001357021.1:c.940+11G>A NP_001343950.1:p.=
NM_001963.5:c.940+11G>A NP_001954.2:p.=
XM_017007845.1:c.964+11G>A XP_016863334.1:p.=
XM_017007846.1:c.964+11G>A XP_016863335.1:p.=
XM_017007847.1:c.964+11G>A XP_016863336.1:p.=
XM_017007848.1:c.964+11G>A XP_016863337.1:p.=
XM_017007849.1:c.964+11G>A XP_016863338.1:p.=
XM_017007850.1:c.964+11G>A XP_016863339.1:p.=
XM_017007851.1:c.964+11G>A XP_016863340.1:p.=
XM_017007853.1:c.964+11G>A XP_016863342.1:p.=
XM_017007854.1:c.964+11G>A XP_016863343.1:p.=
XM_017007855.1:c.964+11G>A XP_016863344.1:p.=
XR_001741156.1:n.1417+11G>A
XR_001741157.1:n.1417+11G>A
NM_001178130.3:c.940+11G>A NP_001171601.1:p.=
NM_001178131.3:c.940+11G>A NP_001171602.1:p.=
NM_001357021.2:c.940+11G>A NP_001343950.1:p.=
NM_001963.6:c.940+11G>A MANE Select NP_001954.2:p.=