Canonical Allele Identifier: CA1484811031

Gene: EGF

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109980901C= , CM000666.2:g.109980901C=	GRCh38
NC_000004.11:g.110902057C= , CM000666.1:g.110902057C=	GRCh37
NC_000004.10:g.111121506C=	NCBI36
NG_011441.1:g.73018C=
NG_011441.2:g.73018C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.2297C= MANE Select	ENSP00000265171.5:p.Ser766=
ENST00000652245.1:c.2171C=	ENSP00000498337.1:p.Ser724=
ENST00000265171.9:c.2297C=	ENSP00000265171.5:p.Ser766=
ENST00000503392.1:c.2297C=	ENSP00000421384.1:p.Ser766=
ENST00000509793.5:c.2171C=	ENSP00000424316.1:p.Ser724=
ENST00000509996.1:n.225C=
ENST00000511228.5:n.261C=
NM_001178130.1:c.2297C=	NP_001171601.1:p.Ser766=
NM_001178131.1:c.2171C=	NP_001171602.1:p.Ser724=
NM_001963.4:c.2297C=	NP_001954.2:p.Ser766=
XM_005262796.2:c.2297C=	XP_005262853.1:p.Ser766=
XM_005262797.2:c.2171C=	XP_005262854.1:p.Ser724=
XM_005262798.2:c.2297C=	XP_005262855.1:p.Ser766=
XM_005262800.2:c.2297C=	XP_005262857.1:p.Ser766=
XM_005262801.2:c.2297C=	XP_005262858.1:p.Ser766=
XM_006714124.2:c.2297C=	XP_006714187.1:p.Ser766=
XM_011531707.1:c.2186C=	XP_011530009.1:p.Ser729=
XM_011531708.1:c.2297C=	XP_011530010.1:p.Ser766=
XR_427532.2:n.2750C=
XR_938699.1:n.2750C=
NM_001178130.2:c.2297C=	NP_001171601.1:p.Ser766=
NM_001178131.2:c.2171C=	NP_001171602.1:p.Ser724=
NM_001357021.1:c.2171C=	NP_001343950.1:p.Ser724=
NM_001963.5:c.2297C=	NP_001954.2:p.Ser766=
XM_017007845.1:c.2321C=	XP_016863334.1:p.Ser774=
XM_017007846.1:c.2321C=	XP_016863335.1:p.Ser774=
XM_017007847.1:c.2321C=	XP_016863336.1:p.Ser774=
XM_017007848.1:c.2195C=	XP_016863337.1:p.Ser732=
XM_017007849.1:c.2321C=	XP_016863338.1:p.Ser774=
XM_017007850.1:c.2321C=	XP_016863339.1:p.Ser774=
XM_017007851.1:c.2321C=	XP_016863340.1:p.Ser774=
XM_017007853.1:c.2321C=	XP_016863342.1:p.Ser774=
XR_001741156.1:n.2774C=
XR_001741157.1:n.2774C=
NM_001178130.3:c.2297C=	NP_001171601.1:p.Ser766=
NM_001178131.3:c.2171C=	NP_001171602.1:p.Ser724=
NM_001357021.2:c.2171C=	NP_001343950.1:p.Ser724=
NM_001963.6:c.2297C= MANE Select	NP_001954.2:p.Ser766=