Canonical Allele Identifier: CA357874654

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925707T>G (hg19) ; chr4:g.110004551T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004551T>G , CM000666.2:g.110004551T>G	GRCh38
NC_000004.11:g.110925707T>G , CM000666.1:g.110925707T>G	GRCh37
NC_000004.10:g.111145156T>G	NCBI36
NG_011441.1:g.96668T>G
NG_011441.2:g.96668T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3220T>G MANE Select	ENSP00000265171.5:p.Ser1074Ala
ENST00000652245.1:c.2851T>G	ENSP00000498337.1:p.Ser951Ala
ENST00000265171.9:c.3220T>G	ENSP00000265171.5:p.Ser1074Ala
ENST00000503392.1:c.3097T>G	ENSP00000421384.1:p.Ser1033Ala
ENST00000509793.5:c.3094T>G	ENSP00000424316.1:p.Ser1032Ala
ENST00000509996.1:n.905T>G
ENST00000537316.5:n.51T>G
ENST00000540840.1:n.51T>G
ENST00000544918.1:n.305T>G
NM_001178130.1:c.3097T>G	NP_001171601.1:p.Ser1033Ala
NM_001178131.1:c.3094T>G	NP_001171602.1:p.Ser1032Ala
NM_001963.4:c.3220T>G	NP_001954.2:p.Ser1074Ala
XM_005262796.2:c.3220T>G	XP_005262853.1:p.Ser1074Ala
XM_005262797.2:c.3094T>G	XP_005262854.1:p.Ser1032Ala
XM_005262798.2:c.2977T>G	XP_005262855.1:p.Ser993Ala
XM_005262800.2:c.2977T>G	XP_005262857.1:p.Ser993Ala
XM_005262801.2:c.2492-6651T>G	XP_005262858.1:n.2492-6651T>G
XM_006714124.2:c.3220T>G	XP_006714187.1:p.Ser1074Ala
XM_011531707.1:c.3109T>G	XP_011530009.1:p.Ser1037Ala
XR_427532.2:n.3234T>G
XR_938699.1:n.3234T>G
NM_001178130.2:c.3097T>G	NP_001171601.1:p.Ser1033Ala
NM_001178131.2:c.3094T>G	NP_001171602.1:p.Ser1032Ala
NM_001357021.1:c.2851T>G	NP_001343950.1:p.Ser951Ala
NM_001963.5:c.3220T>G	NP_001954.2:p.Ser1074Ala
XM_017007845.1:c.3244T>G	XP_016863334.1:p.Ser1082Ala
XM_017007846.1:c.3244T>G	XP_016863335.1:p.Ser1082Ala
XM_017007847.1:c.3121T>G	XP_016863336.1:p.Ser1041Ala
XM_017007848.1:c.3118T>G	XP_016863337.1:p.Ser1040Ala
XM_017007849.1:c.3001T>G	XP_016863338.1:p.Ser1001Ala
XM_017007850.1:c.3244T>G	XP_016863339.1:p.Ser1082Ala
XM_017007851.1:c.3001T>G	XP_016863340.1:p.Ser1001Ala
XR_001741156.1:n.3258T>G
XR_001741157.1:n.3258T>G
NM_001178130.3:c.3097T>G	NP_001171601.1:p.Ser1033Ala
NM_001178131.3:c.3094T>G	NP_001171602.1:p.Ser1032Ala
NM_001357021.2:c.2851T>G	NP_001343950.1:p.Ser951Ala
NM_001963.6:c.3220T>G MANE Select	NP_001954.2:p.Ser1074Ala