Canonical Allele Identifier: CA357874671

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925715A>T (hg19) ; chr4:g.110004559A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004559A>T , CM000666.2:g.110004559A>T	GRCh38
NC_000004.11:g.110925715A>T , CM000666.1:g.110925715A>T	GRCh37
NC_000004.10:g.111145164A>T	NCBI36
NG_011441.1:g.96676A>T
NG_011441.2:g.96676A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3228A>T MANE Select	ENSP00000265171.5:p.Arg1076Ser
ENST00000652245.1:c.2859A>T	ENSP00000498337.1:p.Arg953Ser
ENST00000265171.9:c.3228A>T	ENSP00000265171.5:p.Arg1076Ser
ENST00000503392.1:c.3105A>T	ENSP00000421384.1:p.Arg1035Ser
ENST00000509793.5:c.3102A>T	ENSP00000424316.1:p.Arg1034Ser
ENST00000509996.1:n.913A>T
ENST00000537316.5:n.59A>T
ENST00000540840.1:n.59A>T
ENST00000544918.1:n.313A>T
NM_001178130.1:c.3105A>T	NP_001171601.1:p.Arg1035Ser
NM_001178131.1:c.3102A>T	NP_001171602.1:p.Arg1034Ser
NM_001963.4:c.3228A>T	NP_001954.2:p.Arg1076Ser
XM_005262796.2:c.3228A>T	XP_005262853.1:p.Arg1076Ser
XM_005262797.2:c.3102A>T	XP_005262854.1:p.Arg1034Ser
XM_005262798.2:c.2985A>T	XP_005262855.1:p.Arg995Ser
XM_005262800.2:c.2985A>T	XP_005262857.1:p.Arg995Ser
XM_005262801.2:c.2492-6643A>T	XP_005262858.1:n.2492-6643A>T
XM_006714124.2:c.3228A>T	XP_006714187.1:p.Arg1076Ser
XM_011531707.1:c.3117A>T	XP_011530009.1:p.Arg1039Ser
XR_427532.2:n.3242A>T
XR_938699.1:n.3242A>T
NM_001178130.2:c.3105A>T	NP_001171601.1:p.Arg1035Ser
NM_001178131.2:c.3102A>T	NP_001171602.1:p.Arg1034Ser
NM_001357021.1:c.2859A>T	NP_001343950.1:p.Arg953Ser
NM_001963.5:c.3228A>T	NP_001954.2:p.Arg1076Ser
XM_017007845.1:c.3252A>T	XP_016863334.1:p.Arg1084Ser
XM_017007846.1:c.3252A>T	XP_016863335.1:p.Arg1084Ser
XM_017007847.1:c.3129A>T	XP_016863336.1:p.Arg1043Ser
XM_017007848.1:c.3126A>T	XP_016863337.1:p.Arg1042Ser
XM_017007849.1:c.3009A>T	XP_016863338.1:p.Arg1003Ser
XM_017007850.1:c.3252A>T	XP_016863339.1:p.Arg1084Ser
XM_017007851.1:c.3009A>T	XP_016863340.1:p.Arg1003Ser
XR_001741156.1:n.3266A>T
XR_001741157.1:n.3266A>T
NM_001178130.3:c.3105A>T	NP_001171601.1:p.Arg1035Ser
NM_001178131.3:c.3102A>T	NP_001171602.1:p.Arg1034Ser
NM_001357021.2:c.2859A>T	NP_001343950.1:p.Arg953Ser
NM_001963.6:c.3228A>T MANE Select	NP_001954.2:p.Arg1076Ser