Canonical Allele Identifier: CA440594005

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110902049T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109980893T>G , CM000666.2:g.109980893T>G	GRCh38
NC_000004.11:g.110902049T>G , CM000666.1:g.110902049T>G	GRCh37
NC_000004.10:g.111121498T>G	NCBI36
NG_011441.1:g.73010T>G
NG_011441.2:g.73010T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.2289T>G MANE Select	ENSP00000265171.5:p.Ala763=
ENST00000652245.1:c.2163T>G	ENSP00000498337.1:p.Ala721=
ENST00000265171.9:c.2289T>G	ENSP00000265171.5:p.Ala763=
ENST00000503392.1:c.2289T>G	ENSP00000421384.1:p.Ala763=
ENST00000509793.5:c.2163T>G	ENSP00000424316.1:p.Ala721=
ENST00000509996.1:n.217T>G
ENST00000511228.5:n.253T>G
NM_001178130.1:c.2289T>G	NP_001171601.1:p.Ala763=
NM_001178131.1:c.2163T>G	NP_001171602.1:p.Ala721=
NM_001963.4:c.2289T>G	NP_001954.2:p.Ala763=
XM_005262796.2:c.2289T>G	XP_005262853.1:p.Ala763=
XM_005262797.2:c.2163T>G	XP_005262854.1:p.Ala721=
XM_005262798.2:c.2289T>G	XP_005262855.1:p.Ala763=
XM_005262800.2:c.2289T>G	XP_005262857.1:p.Ala763=
XM_005262801.2:c.2289T>G	XP_005262858.1:p.Ala763=
XM_006714124.2:c.2289T>G	XP_006714187.1:p.Ala763=
XM_011531707.1:c.2178T>G	XP_011530009.1:p.Ala726=
XM_011531708.1:c.2289T>G	XP_011530010.1:p.Ala763=
XR_427532.2:n.2742T>G
XR_938699.1:n.2742T>G
NM_001178130.2:c.2289T>G	NP_001171601.1:p.Ala763=
NM_001178131.2:c.2163T>G	NP_001171602.1:p.Ala721=
NM_001357021.1:c.2163T>G	NP_001343950.1:p.Ala721=
NM_001963.5:c.2289T>G	NP_001954.2:p.Ala763=
XM_017007845.1:c.2313T>G	XP_016863334.1:p.Ala771=
XM_017007846.1:c.2313T>G	XP_016863335.1:p.Ala771=
XM_017007847.1:c.2313T>G	XP_016863336.1:p.Ala771=
XM_017007848.1:c.2187T>G	XP_016863337.1:p.Ala729=
XM_017007849.1:c.2313T>G	XP_016863338.1:p.Ala771=
XM_017007850.1:c.2313T>G	XP_016863339.1:p.Ala771=
XM_017007851.1:c.2313T>G	XP_016863340.1:p.Ala771=
XM_017007853.1:c.2313T>G	XP_016863342.1:p.Ala771=
XR_001741156.1:n.2766T>G
XR_001741157.1:n.2766T>G
NM_001178130.3:c.2289T>G	NP_001171601.1:p.Ala763=
NM_001178131.3:c.2163T>G	NP_001171602.1:p.Ala721=
NM_001357021.2:c.2163T>G	NP_001343950.1:p.Ala721=
NM_001963.6:c.2289T>G MANE Select	NP_001954.2:p.Ala763=