Canonical Allele Identifier: CA357874659

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925710A>C (hg19) ; chr4:g.110004554A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004554A>C , CM000666.2:g.110004554A>C	GRCh38
NC_000004.11:g.110925710A>C , CM000666.1:g.110925710A>C	GRCh37
NC_000004.10:g.111145159A>C	NCBI36
NG_011441.1:g.96671A>C
NG_011441.2:g.96671A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.3223A>C MANE Select	ENSP00000265171.5:p.Ser1075Arg
ENST00000652245.1:c.2854A>C	ENSP00000498337.1:p.Ser952Arg
ENST00000265171.9:c.3223A>C	ENSP00000265171.5:p.Ser1075Arg
ENST00000503392.1:c.3100A>C	ENSP00000421384.1:p.Ser1034Arg
ENST00000509793.5:c.3097A>C	ENSP00000424316.1:p.Ser1033Arg
ENST00000509996.1:n.908A>C
ENST00000537316.5:n.54A>C
ENST00000540840.1:n.54A>C
ENST00000544918.1:n.308A>C
NM_001178130.1:c.3100A>C	NP_001171601.1:p.Ser1034Arg
NM_001178131.1:c.3097A>C	NP_001171602.1:p.Ser1033Arg
NM_001963.4:c.3223A>C	NP_001954.2:p.Ser1075Arg
XM_005262796.2:c.3223A>C	XP_005262853.1:p.Ser1075Arg
XM_005262797.2:c.3097A>C	XP_005262854.1:p.Ser1033Arg
XM_005262798.2:c.2980A>C	XP_005262855.1:p.Ser994Arg
XM_005262800.2:c.2980A>C	XP_005262857.1:p.Ser994Arg
XM_005262801.2:c.2492-6648A>C	XP_005262858.1:n.2492-6648A>C
XM_006714124.2:c.3223A>C	XP_006714187.1:p.Ser1075Arg
XM_011531707.1:c.3112A>C	XP_011530009.1:p.Ser1038Arg
XR_427532.2:n.3237A>C
XR_938699.1:n.3237A>C
NM_001178130.2:c.3100A>C	NP_001171601.1:p.Ser1034Arg
NM_001178131.2:c.3097A>C	NP_001171602.1:p.Ser1033Arg
NM_001357021.1:c.2854A>C	NP_001343950.1:p.Ser952Arg
NM_001963.5:c.3223A>C	NP_001954.2:p.Ser1075Arg
XM_017007845.1:c.3247A>C	XP_016863334.1:p.Ser1083Arg
XM_017007846.1:c.3247A>C	XP_016863335.1:p.Ser1083Arg
XM_017007847.1:c.3124A>C	XP_016863336.1:p.Ser1042Arg
XM_017007848.1:c.3121A>C	XP_016863337.1:p.Ser1041Arg
XM_017007849.1:c.3004A>C	XP_016863338.1:p.Ser1002Arg
XM_017007850.1:c.3247A>C	XP_016863339.1:p.Ser1083Arg
XM_017007851.1:c.3004A>C	XP_016863340.1:p.Ser1002Arg
XR_001741156.1:n.3261A>C
XR_001741157.1:n.3261A>C
NM_001178130.3:c.3100A>C	NP_001171601.1:p.Ser1034Arg
NM_001178131.3:c.3097A>C	NP_001171602.1:p.Ser1033Arg
NM_001357021.2:c.2854A>C	NP_001343950.1:p.Ser952Arg
NM_001963.6:c.3223A>C MANE Select	NP_001954.2:p.Ser1075Arg