Canonical Allele Identifier: CA440593645

Gene: EGF

Linked Data

• MyVariant Identifiers: chr4:g.110925697T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110004541T>G , CM000666.2:g.110004541T>G	GRCh38
NC_000004.11:g.110925697T>G , CM000666.1:g.110925697T>G	GRCh37
NC_000004.10:g.111145146T>G	NCBI36
NG_011441.1:g.96658T>G
NG_011441.2:g.96658T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265171.10:c.3210T>G MANE Select	ENSP00000265171.5:p.Pro1070=
ENST00000652245.1:c.2841T>G	ENSP00000498337.1:p.Pro947=
ENST00000265171.9:c.3210T>G	ENSP00000265171.5:p.Pro1070=
ENST00000503392.1:c.3087T>G	ENSP00000421384.1:p.Pro1029=
ENST00000509793.5:c.3084T>G	ENSP00000424316.1:p.Pro1028=
ENST00000509996.1:n.895T>G
ENST00000537316.5:n.41T>G
ENST00000540840.1:n.41T>G
ENST00000544918.1:n.295T>G
NM_001178130.1:c.3087T>G	NP_001171601.1:p.Pro1029=
NM_001178131.1:c.3084T>G	NP_001171602.1:p.Pro1028=
NM_001963.4:c.3210T>G	NP_001954.2:p.Pro1070=
XM_005262796.2:c.3210T>G	XP_005262853.1:p.Pro1070=
XM_005262797.2:c.3084T>G	XP_005262854.1:p.Pro1028=
XM_005262798.2:c.2967T>G	XP_005262855.1:p.Pro989=
XM_005262800.2:c.2967T>G	XP_005262857.1:p.Pro989=
XM_005262801.2:c.2492-6661T>G	XP_005262858.1:n.2492-6661T>G
XM_006714124.2:c.3210T>G	XP_006714187.1:p.Pro1070=
XM_011531707.1:c.3099T>G	XP_011530009.1:p.Pro1033=
XR_427532.2:n.3224T>G
XR_938699.1:n.3224T>G
NM_001178130.2:c.3087T>G	NP_001171601.1:p.Pro1029=
NM_001178131.2:c.3084T>G	NP_001171602.1:p.Pro1028=
NM_001357021.1:c.2841T>G	NP_001343950.1:p.Pro947=
NM_001963.5:c.3210T>G	NP_001954.2:p.Pro1070=
XM_017007845.1:c.3234T>G	XP_016863334.1:p.Pro1078=
XM_017007846.1:c.3234T>G	XP_016863335.1:p.Pro1078=
XM_017007847.1:c.3111T>G	XP_016863336.1:p.Pro1037=
XM_017007848.1:c.3108T>G	XP_016863337.1:p.Pro1036=
XM_017007849.1:c.2991T>G	XP_016863338.1:p.Pro997=
XM_017007850.1:c.3234T>G	XP_016863339.1:p.Pro1078=
XM_017007851.1:c.2991T>G	XP_016863340.1:p.Pro997=
XR_001741156.1:n.3248T>G
XR_001741157.1:n.3248T>G
NM_001178130.3:c.3087T>G	NP_001171601.1:p.Pro1029=
NM_001178131.3:c.3084T>G	NP_001171602.1:p.Pro1028=
NM_001357021.2:c.2841T>G	NP_001343950.1:p.Pro947=
NM_001963.6:c.3210T>G MANE Select	NP_001954.2:p.Pro1070=