Canonical Allele Identifier: CA357874638

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925701G>T (hg19) ; chr4:g.110004545G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004545G>T , CM000666.2:g.110004545G>T	GRCh38
NC_000004.11:g.110925701G>T , CM000666.1:g.110925701G>T	GRCh37
NC_000004.10:g.111145150G>T	NCBI36
NG_011441.1:g.96662G>T
NG_011441.2:g.96662G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3214G>T MANE Select	ENSP00000265171.5:p.Glu1072Ter
ENST00000652245.1:c.2845G>T	ENSP00000498337.1:p.Glu949Ter
ENST00000265171.9:c.3214G>T	ENSP00000265171.5:p.Glu1072Ter
ENST00000503392.1:c.3091G>T	ENSP00000421384.1:p.Glu1031Ter
ENST00000509793.5:c.3088G>T	ENSP00000424316.1:p.Glu1030Ter
ENST00000509996.1:n.899G>T
ENST00000537316.5:n.45G>T
ENST00000540840.1:n.45G>T
ENST00000544918.1:n.299G>T
NM_001178130.1:c.3091G>T	NP_001171601.1:p.Glu1031Ter
NM_001178131.1:c.3088G>T	NP_001171602.1:p.Glu1030Ter
NM_001963.4:c.3214G>T	NP_001954.2:p.Glu1072Ter
XM_005262796.2:c.3214G>T	XP_005262853.1:p.Glu1072Ter
XM_005262797.2:c.3088G>T	XP_005262854.1:p.Glu1030Ter
XM_005262798.2:c.2971G>T	XP_005262855.1:p.Glu991Ter
XM_005262800.2:c.2971G>T	XP_005262857.1:p.Glu991Ter
XM_005262801.2:c.2492-6657G>T	XP_005262858.1:n.2492-6657G>T
XM_006714124.2:c.3214G>T	XP_006714187.1:p.Glu1072Ter
XM_011531707.1:c.3103G>T	XP_011530009.1:p.Glu1035Ter
XR_427532.2:n.3228G>T
XR_938699.1:n.3228G>T
NM_001178130.2:c.3091G>T	NP_001171601.1:p.Glu1031Ter
NM_001178131.2:c.3088G>T	NP_001171602.1:p.Glu1030Ter
NM_001357021.1:c.2845G>T	NP_001343950.1:p.Glu949Ter
NM_001963.5:c.3214G>T	NP_001954.2:p.Glu1072Ter
XM_017007845.1:c.3238G>T	XP_016863334.1:p.Glu1080Ter
XM_017007846.1:c.3238G>T	XP_016863335.1:p.Glu1080Ter
XM_017007847.1:c.3115G>T	XP_016863336.1:p.Glu1039Ter
XM_017007848.1:c.3112G>T	XP_016863337.1:p.Glu1038Ter
XM_017007849.1:c.2995G>T	XP_016863338.1:p.Glu999Ter
XM_017007850.1:c.3238G>T	XP_016863339.1:p.Glu1080Ter
XM_017007851.1:c.2995G>T	XP_016863340.1:p.Glu999Ter
XR_001741156.1:n.3252G>T
XR_001741157.1:n.3252G>T
NM_001178130.3:c.3091G>T	NP_001171601.1:p.Glu1031Ter
NM_001178131.3:c.3088G>T	NP_001171602.1:p.Glu1030Ter
NM_001357021.2:c.2845G>T	NP_001343950.1:p.Glu949Ter
NM_001963.6:c.3214G>T MANE Select	NP_001954.2:p.Glu1072Ter