Canonical Allele Identifier: CA440593662

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925712C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004556C>T , CM000666.2:g.110004556C>T	GRCh38
NC_000004.11:g.110925712C>T , CM000666.1:g.110925712C>T	GRCh37
NC_000004.10:g.111145161C>T	NCBI36
NG_011441.1:g.96673C>T
NG_011441.2:g.96673C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3225C>T MANE Select	ENSP00000265171.5:p.Ser1075=
ENST00000652245.1:c.2856C>T	ENSP00000498337.1:p.Ser952=
ENST00000265171.9:c.3225C>T	ENSP00000265171.5:p.Ser1075=
ENST00000503392.1:c.3102C>T	ENSP00000421384.1:p.Ser1034=
ENST00000509793.5:c.3099C>T	ENSP00000424316.1:p.Ser1033=
ENST00000509996.1:n.910C>T
ENST00000537316.5:n.56C>T
ENST00000540840.1:n.56C>T
ENST00000544918.1:n.310C>T
NM_001178130.1:c.3102C>T	NP_001171601.1:p.Ser1034=
NM_001178131.1:c.3099C>T	NP_001171602.1:p.Ser1033=
NM_001963.4:c.3225C>T	NP_001954.2:p.Ser1075=
XM_005262796.2:c.3225C>T	XP_005262853.1:p.Ser1075=
XM_005262797.2:c.3099C>T	XP_005262854.1:p.Ser1033=
XM_005262798.2:c.2982C>T	XP_005262855.1:p.Ser994=
XM_005262800.2:c.2982C>T	XP_005262857.1:p.Ser994=
XM_005262801.2:c.2492-6646C>T	XP_005262858.1:n.2492-6646C>T
XM_006714124.2:c.3225C>T	XP_006714187.1:p.Ser1075=
XM_011531707.1:c.3114C>T	XP_011530009.1:p.Ser1038=
XR_427532.2:n.3239C>T
XR_938699.1:n.3239C>T
NM_001178130.2:c.3102C>T	NP_001171601.1:p.Ser1034=
NM_001178131.2:c.3099C>T	NP_001171602.1:p.Ser1033=
NM_001357021.1:c.2856C>T	NP_001343950.1:p.Ser952=
NM_001963.5:c.3225C>T	NP_001954.2:p.Ser1075=
XM_017007845.1:c.3249C>T	XP_016863334.1:p.Ser1083=
XM_017007846.1:c.3249C>T	XP_016863335.1:p.Ser1083=
XM_017007847.1:c.3126C>T	XP_016863336.1:p.Ser1042=
XM_017007848.1:c.3123C>T	XP_016863337.1:p.Ser1041=
XM_017007849.1:c.3006C>T	XP_016863338.1:p.Ser1002=
XM_017007850.1:c.3249C>T	XP_016863339.1:p.Ser1083=
XM_017007851.1:c.3006C>T	XP_016863340.1:p.Ser1002=
XR_001741156.1:n.3263C>T
XR_001741157.1:n.3263C>T
NM_001178130.3:c.3102C>T	NP_001171601.1:p.Ser1034=
NM_001178131.3:c.3099C>T	NP_001171602.1:p.Ser1033=
NM_001357021.2:c.2856C>T	NP_001343950.1:p.Ser952=
NM_001963.6:c.3225C>T MANE Select	NP_001954.2:p.Ser1075=