Canonical Allele Identifier: CA1484810925

Gene: EGF

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109980838_109980840delinsGCT , CM000666.2:g.109980838_109980840delinsGCT	GRCh38
NC_000004.11:g.110901994_110901996delinsGCT , CM000666.1:g.110901994_110901996delinsGCT	GRCh37
NC_000004.10:g.111121443_111121445delinsGCT	NCBI36
NG_011441.1:g.72955_72957delinsGCT
NG_011441.2:g.72955_72957delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.2234_2236delinsGCT MANE Select	ENSP00000265171.5:p.Cys745=
ENST00000652245.1:c.2108_2110delinsGCT	ENSP00000498337.1:p.Cys703=
ENST00000265171.9:c.2234_2236delinsGCT	ENSP00000265171.5:p.Cys745=
ENST00000503392.1:c.2234_2236delinsGCT	ENSP00000421384.1:p.Cys745=
ENST00000509793.5:c.2108_2110delinsGCT	ENSP00000424316.1:p.Cys703=
ENST00000509996.1:n.162_164delinsGCT
ENST00000511228.5:n.198_200delinsGCT
NM_001178130.1:c.2234_2236delinsGCT	NP_001171601.1:p.Cys745=
NM_001178131.1:c.2108_2110delinsGCT	NP_001171602.1:p.Cys703=
NM_001963.4:c.2234_2236delinsGCT	NP_001954.2:p.Cys745=
XM_005262796.2:c.2234_2236delinsGCT	XP_005262853.1:p.Cys745=
XM_005262797.2:c.2108_2110delinsGCT	XP_005262854.1:p.Cys703=
XM_005262798.2:c.2234_2236delinsGCT	XP_005262855.1:p.Cys745=
XM_005262800.2:c.2234_2236delinsGCT	XP_005262857.1:p.Cys745=
XM_005262801.2:c.2234_2236delinsGCT	XP_005262858.1:p.Cys745=
XM_006714124.2:c.2234_2236delinsGCT	XP_006714187.1:p.Cys745=
XM_011531707.1:c.2123_2125delinsGCT	XP_011530009.1:p.Cys708=
XM_011531708.1:c.2234_2236delinsGCT	XP_011530010.1:p.Cys745=
XR_427532.2:n.2687_2689delinsGCT
XR_938699.1:n.2687_2689delinsGCT
NM_001178130.2:c.2234_2236delinsGCT	NP_001171601.1:p.Cys745=
NM_001178131.2:c.2108_2110delinsGCT	NP_001171602.1:p.Cys703=
NM_001357021.1:c.2108_2110delinsGCT	NP_001343950.1:p.Cys703=
NM_001963.5:c.2234_2236delinsGCT	NP_001954.2:p.Cys745=
XM_017007845.1:c.2258_2260delinsGCT	XP_016863334.1:p.Cys753=
XM_017007846.1:c.2258_2260delinsGCT	XP_016863335.1:p.Cys753=
XM_017007847.1:c.2258_2260delinsGCT	XP_016863336.1:p.Cys753=
XM_017007848.1:c.2132_2134delinsGCT	XP_016863337.1:p.Cys711=
XM_017007849.1:c.2258_2260delinsGCT	XP_016863338.1:p.Cys753=
XM_017007850.1:c.2258_2260delinsGCT	XP_016863339.1:p.Cys753=
XM_017007851.1:c.2258_2260delinsGCT	XP_016863340.1:p.Cys753=
XM_017007853.1:c.2258_2260delinsGCT	XP_016863342.1:p.Cys753=
XR_001741156.1:n.2711_2713delinsGCT
XR_001741157.1:n.2711_2713delinsGCT
NM_001178130.3:c.2234_2236delinsGCT	NP_001171601.1:p.Cys745=
NM_001178131.3:c.2108_2110delinsGCT	NP_001171602.1:p.Cys703=
NM_001357021.2:c.2108_2110delinsGCT	NP_001343950.1:p.Cys703=
NM_001963.6:c.2234_2236delinsGCT MANE Select	NP_001954.2:p.Cys745=