Canonical Allele Identifier: CA357874666

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925713A>T (hg19) ; chr4:g.110004557A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004557A>T , CM000666.2:g.110004557A>T	GRCh38
NC_000004.11:g.110925713A>T , CM000666.1:g.110925713A>T	GRCh37
NC_000004.10:g.111145162A>T	NCBI36
NG_011441.1:g.96674A>T
NG_011441.2:g.96674A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.3226A>T MANE Select	ENSP00000265171.5:p.Arg1076Ter
ENST00000652245.1:c.2857A>T	ENSP00000498337.1:p.Arg953Ter
ENST00000265171.9:c.3226A>T	ENSP00000265171.5:p.Arg1076Ter
ENST00000503392.1:c.3103A>T	ENSP00000421384.1:p.Arg1035Ter
ENST00000509793.5:c.3100A>T	ENSP00000424316.1:p.Arg1034Ter
ENST00000509996.1:n.911A>T
ENST00000537316.5:n.57A>T
ENST00000540840.1:n.57A>T
ENST00000544918.1:n.311A>T
NM_001178130.1:c.3103A>T	NP_001171601.1:p.Arg1035Ter
NM_001178131.1:c.3100A>T	NP_001171602.1:p.Arg1034Ter
NM_001963.4:c.3226A>T	NP_001954.2:p.Arg1076Ter
XM_005262796.2:c.3226A>T	XP_005262853.1:p.Arg1076Ter
XM_005262797.2:c.3100A>T	XP_005262854.1:p.Arg1034Ter
XM_005262798.2:c.2983A>T	XP_005262855.1:p.Arg995Ter
XM_005262800.2:c.2983A>T	XP_005262857.1:p.Arg995Ter
XM_005262801.2:c.2492-6645A>T	XP_005262858.1:n.2492-6645A>T
XM_006714124.2:c.3226A>T	XP_006714187.1:p.Arg1076Ter
XM_011531707.1:c.3115A>T	XP_011530009.1:p.Arg1039Ter
XR_427532.2:n.3240A>T
XR_938699.1:n.3240A>T
NM_001178130.2:c.3103A>T	NP_001171601.1:p.Arg1035Ter
NM_001178131.2:c.3100A>T	NP_001171602.1:p.Arg1034Ter
NM_001357021.1:c.2857A>T	NP_001343950.1:p.Arg953Ter
NM_001963.5:c.3226A>T	NP_001954.2:p.Arg1076Ter
XM_017007845.1:c.3250A>T	XP_016863334.1:p.Arg1084Ter
XM_017007846.1:c.3250A>T	XP_016863335.1:p.Arg1084Ter
XM_017007847.1:c.3127A>T	XP_016863336.1:p.Arg1043Ter
XM_017007848.1:c.3124A>T	XP_016863337.1:p.Arg1042Ter
XM_017007849.1:c.3007A>T	XP_016863338.1:p.Arg1003Ter
XM_017007850.1:c.3250A>T	XP_016863339.1:p.Arg1084Ter
XM_017007851.1:c.3007A>T	XP_016863340.1:p.Arg1003Ter
XR_001741156.1:n.3264A>T
XR_001741157.1:n.3264A>T
NM_001178130.3:c.3103A>T	NP_001171601.1:p.Arg1035Ter
NM_001178131.3:c.3100A>T	NP_001171602.1:p.Arg1034Ter
NM_001357021.2:c.2857A>T	NP_001343950.1:p.Arg953Ter
NM_001963.6:c.3226A>T MANE Select	NP_001954.2:p.Arg1076Ter