Canonical Allele Identifier: CA1484809965

Gene: EGF

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109980042G= , CM000666.2:g.109980042G=	GRCh38
NC_000004.11:g.110901198G= , CM000666.1:g.110901198G=	GRCh37
NC_000004.10:g.111120647G=	NCBI36
NG_011441.1:g.72159G=
NG_011441.2:g.72159G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.2124G= MANE Select	ENSP00000265171.5:p.Met708=
ENST00000652245.1:c.1998G=	ENSP00000498337.1:p.Met666=
ENST00000265171.9:c.2124G=	ENSP00000265171.5:p.Met708=
ENST00000503392.1:c.2124G=	ENSP00000421384.1:p.Met708=
ENST00000509793.5:c.1998G=	ENSP00000424316.1:p.Met666=
NM_001178130.1:c.2124G=	NP_001171601.1:p.Met708=
NM_001178131.1:c.1998G=	NP_001171602.1:p.Met666=
NM_001963.4:c.2124G=	NP_001954.2:p.Met708=
XM_005262796.2:c.2124G=	XP_005262853.1:p.Met708=
XM_005262797.2:c.1998G=	XP_005262854.1:p.Met666=
XM_005262798.2:c.2124G=	XP_005262855.1:p.Met708=
XM_005262800.2:c.2124G=	XP_005262857.1:p.Met708=
XM_005262801.2:c.2124G=	XP_005262858.1:p.Met708=
XM_005262802.2:c.*53G=	XP_005262859.1:n.*53G=
XM_006714124.2:c.2124G=	XP_006714187.1:p.Met708=
XM_011531707.1:c.2013G=	XP_011530009.1:p.Met671=
XM_011531708.1:c.2124G=	XP_011530010.1:p.Met708=
XR_427532.2:n.2577G=
XR_938699.1:n.2577G=
NM_001178130.2:c.2124G=	NP_001171601.1:p.Met708=
NM_001178131.2:c.1998G=	NP_001171602.1:p.Met666=
NM_001357021.1:c.1998G=	NP_001343950.1:p.Met666=
NM_001963.5:c.2124G=	NP_001954.2:p.Met708=
XM_017007845.1:c.2148G=	XP_016863334.1:p.Met716=
XM_017007846.1:c.2148G=	XP_016863335.1:p.Met716=
XM_017007847.1:c.2148G=	XP_016863336.1:p.Met716=
XM_017007848.1:c.2022G=	XP_016863337.1:p.Met674=
XM_017007849.1:c.2148G=	XP_016863338.1:p.Met716=
XM_017007850.1:c.2148G=	XP_016863339.1:p.Met716=
XM_017007851.1:c.2148G=	XP_016863340.1:p.Met716=
XM_017007853.1:c.2148G=	XP_016863342.1:p.Met716=
XM_017007855.1:c.*53G=	XP_016863344.1:n.*53G=
XR_001741156.1:n.2601G=
XR_001741157.1:n.2601G=
NM_001178130.3:c.2124G=	NP_001171601.1:p.Met708=
NM_001178131.3:c.1998G=	NP_001171602.1:p.Met666=
NM_001357021.2:c.1998G=	NP_001343950.1:p.Met666=
NM_001963.6:c.2124G= MANE Select	NP_001954.2:p.Met708=