Canonical Allele Identifier: CA357874639

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925702A>T (hg19) ; chr4:g.110004546A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004546A>T , CM000666.2:g.110004546A>T	GRCh38
NC_000004.11:g.110925702A>T , CM000666.1:g.110925702A>T	GRCh37
NC_000004.10:g.111145151A>T	NCBI36
NG_011441.1:g.96663A>T
NG_011441.2:g.96663A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3215A>T MANE Select	ENSP00000265171.5:p.Glu1072Val
ENST00000652245.1:c.2846A>T	ENSP00000498337.1:p.Glu949Val
ENST00000265171.9:c.3215A>T	ENSP00000265171.5:p.Glu1072Val
ENST00000503392.1:c.3092A>T	ENSP00000421384.1:p.Glu1031Val
ENST00000509793.5:c.3089A>T	ENSP00000424316.1:p.Glu1030Val
ENST00000509996.1:n.900A>T
ENST00000537316.5:n.46A>T
ENST00000540840.1:n.46A>T
ENST00000544918.1:n.300A>T
NM_001178130.1:c.3092A>T	NP_001171601.1:p.Glu1031Val
NM_001178131.1:c.3089A>T	NP_001171602.1:p.Glu1030Val
NM_001963.4:c.3215A>T	NP_001954.2:p.Glu1072Val
XM_005262796.2:c.3215A>T	XP_005262853.1:p.Glu1072Val
XM_005262797.2:c.3089A>T	XP_005262854.1:p.Glu1030Val
XM_005262798.2:c.2972A>T	XP_005262855.1:p.Glu991Val
XM_005262800.2:c.2972A>T	XP_005262857.1:p.Glu991Val
XM_005262801.2:c.2492-6656A>T	XP_005262858.1:n.2492-6656A>T
XM_006714124.2:c.3215A>T	XP_006714187.1:p.Glu1072Val
XM_011531707.1:c.3104A>T	XP_011530009.1:p.Glu1035Val
XR_427532.2:n.3229A>T
XR_938699.1:n.3229A>T
NM_001178130.2:c.3092A>T	NP_001171601.1:p.Glu1031Val
NM_001178131.2:c.3089A>T	NP_001171602.1:p.Glu1030Val
NM_001357021.1:c.2846A>T	NP_001343950.1:p.Glu949Val
NM_001963.5:c.3215A>T	NP_001954.2:p.Glu1072Val
XM_017007845.1:c.3239A>T	XP_016863334.1:p.Glu1080Val
XM_017007846.1:c.3239A>T	XP_016863335.1:p.Glu1080Val
XM_017007847.1:c.3116A>T	XP_016863336.1:p.Glu1039Val
XM_017007848.1:c.3113A>T	XP_016863337.1:p.Glu1038Val
XM_017007849.1:c.2996A>T	XP_016863338.1:p.Glu999Val
XM_017007850.1:c.3239A>T	XP_016863339.1:p.Glu1080Val
XM_017007851.1:c.2996A>T	XP_016863340.1:p.Glu999Val
XR_001741156.1:n.3253A>T
XR_001741157.1:n.3253A>T
NM_001178130.3:c.3092A>T	NP_001171601.1:p.Glu1031Val
NM_001178131.3:c.3089A>T	NP_001171602.1:p.Glu1030Val
NM_001357021.2:c.2846A>T	NP_001343950.1:p.Glu949Val
NM_001963.6:c.3215A>T MANE Select	NP_001954.2:p.Glu1072Val