Canonical Allele Identifier: CA357885036

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110902062C>A (hg19) ; chr4:g.109980906C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.2302C>A MANE Select	ENSP00000265171.5:p.Arg768Ser
ENST00000652245.1:c.2176C>A	ENSP00000498337.1:p.Arg726Ser
ENST00000265171.9:c.2302C>A	ENSP00000265171.5:p.Arg768Ser
ENST00000503392.1:c.2302C>A	ENSP00000421384.1:p.Arg768Ser
ENST00000509793.5:c.2176C>A	ENSP00000424316.1:p.Arg726Ser
ENST00000509996.1:n.230C>A
ENST00000511228.5:n.266C>A
NM_001178130.1:c.2302C>A	NP_001171601.1:p.Arg768Ser
NM_001178131.1:c.2176C>A	NP_001171602.1:p.Arg726Ser
NM_001963.4:c.2302C>A	NP_001954.2:p.Arg768Ser
XM_005262796.2:c.2302C>A	XP_005262853.1:p.Arg768Ser
XM_005262797.2:c.2176C>A	XP_005262854.1:p.Arg726Ser
XM_005262798.2:c.2302C>A	XP_005262855.1:p.Arg768Ser
XM_005262800.2:c.2302C>A	XP_005262857.1:p.Arg768Ser
XM_005262801.2:c.2302C>A	XP_005262858.1:p.Arg768Ser
XM_006714124.2:c.2302C>A	XP_006714187.1:p.Arg768Ser
XM_011531707.1:c.2191C>A	XP_011530009.1:p.Arg731Ser
XM_011531708.1:c.2302C>A	XP_011530010.1:p.Arg768Ser
XR_427532.2:n.2755C>A
XR_938699.1:n.2755C>A
NM_001178130.2:c.2302C>A	NP_001171601.1:p.Arg768Ser
NM_001178131.2:c.2176C>A	NP_001171602.1:p.Arg726Ser
NM_001357021.1:c.2176C>A	NP_001343950.1:p.Arg726Ser
NM_001963.5:c.2302C>A	NP_001954.2:p.Arg768Ser
XM_017007845.1:c.2326C>A	XP_016863334.1:p.Arg776Ser
XM_017007846.1:c.2326C>A	XP_016863335.1:p.Arg776Ser
XM_017007847.1:c.2326C>A	XP_016863336.1:p.Arg776Ser
XM_017007848.1:c.2200C>A	XP_016863337.1:p.Arg734Ser
XM_017007849.1:c.2326C>A	XP_016863338.1:p.Arg776Ser
XM_017007850.1:c.2326C>A	XP_016863339.1:p.Arg776Ser
XM_017007851.1:c.2326C>A	XP_016863340.1:p.Arg776Ser
XM_017007853.1:c.2326C>A	XP_016863342.1:p.Arg776Ser
XR_001741156.1:n.2779C>A
XR_001741157.1:n.2779C>A
NM_001178130.3:c.2302C>A	NP_001171601.1:p.Arg768Ser
NM_001178131.3:c.2176C>A	NP_001171602.1:p.Arg726Ser
NM_001357021.2:c.2176C>A	NP_001343950.1:p.Arg726Ser
NM_001963.6:c.2302C>A MANE Select	NP_001954.2:p.Arg768Ser