Canonical Allele Identifier: CA554050861

Gene: EGF

Linked Data

• dbSNP Id: rs1408703133
• gnomAD v2: 4-110866510-TTGTA-T
• gnomAD v3: 4-109945354-TTGTA-T
• gnomAD v4: 4-109945354-TTGTA-T
• MyVariant Identifiers: chr4:g.110866511_110866514del (hg19) ; chr4:g.109945355_109945358del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109945355_109945358del , CM000666.2:g.109945355_109945358del	GRCh38
NC_000004.11:g.110866511_110866514del , CM000666.1:g.110866511_110866514del	GRCh37
NC_000004.10:g.111085960_111085963del	NCBI36
NG_011441.1:g.37472_37475del
NG_011441.2:g.37472_37475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.940+80_940+83del MANE Select	ENSP00000265171.5:n.940+80_940+83del
ENST00000652245.1:c.940+80_940+83del	ENSP00000498337.1:n.940+80_940+83del
ENST00000265171.9:c.940+80_940+83del	ENSP00000265171.5:n.940+80_940+83del
ENST00000503392.1:c.940+80_940+83del	ENSP00000421384.1:n.940+80_940+83del
ENST00000509793.5:c.940+80_940+83del	ENSP00000424316.1:n.940+80_940+83del
NM_001178130.1:c.940+80_940+83del	NP_001171601.1:n.940+80_940+83del
NM_001178131.1:c.940+80_940+83del	NP_001171602.1:n.940+80_940+83del
NM_001963.4:c.940+80_940+83del	NP_001954.2:n.940+80_940+83del
XM_005262796.2:c.940+80_940+83del	XP_005262853.1:n.940+80_940+83del
XM_005262797.2:c.940+80_940+83del	XP_005262854.1:n.940+80_940+83del
XM_005262798.2:c.940+80_940+83del	XP_005262855.1:n.940+80_940+83del
XM_005262800.2:c.940+80_940+83del	XP_005262857.1:n.940+80_940+83del
XM_005262801.2:c.940+80_940+83del	XP_005262858.1:n.940+80_940+83del
XM_005262802.2:c.940+80_940+83del	XP_005262859.1:n.940+80_940+83del
XM_006714124.2:c.940+80_940+83del	XP_006714187.1:n.940+80_940+83del
XM_011531707.1:c.829+80_829+83del	XP_011530009.1:n.829+80_829+83del
XM_011531708.1:c.940+80_940+83del	XP_011530010.1:n.940+80_940+83del
XM_011531709.1:c.940+80_940+83del	XP_011530011.1:n.940+80_940+83del
XR_427532.2:n.1393+80_1393+83del
XR_938699.1:n.1393+80_1393+83del
NM_001178130.2:c.940+80_940+83del	NP_001171601.1:n.940+80_940+83del
NM_001178131.2:c.940+80_940+83del	NP_001171602.1:n.940+80_940+83del
NM_001357021.1:c.940+80_940+83del	NP_001343950.1:n.940+80_940+83del
NM_001963.5:c.940+80_940+83del	NP_001954.2:n.940+80_940+83del
XM_017007845.1:c.964+80_964+83del	XP_016863334.1:n.964+80_964+83del
XM_017007846.1:c.964+80_964+83del	XP_016863335.1:n.964+80_964+83del
XM_017007847.1:c.964+80_964+83del	XP_016863336.1:n.964+80_964+83del
XM_017007848.1:c.964+80_964+83del	XP_016863337.1:n.964+80_964+83del
XM_017007849.1:c.964+80_964+83del	XP_016863338.1:n.964+80_964+83del
XM_017007850.1:c.964+80_964+83del	XP_016863339.1:n.964+80_964+83del
XM_017007851.1:c.964+80_964+83del	XP_016863340.1:n.964+80_964+83del
XM_017007853.1:c.964+80_964+83del	XP_016863342.1:n.964+80_964+83del
XM_017007854.1:c.964+80_964+83del	XP_016863343.1:n.964+80_964+83del
XM_017007855.1:c.964+80_964+83del	XP_016863344.1:n.964+80_964+83del
XR_001741156.1:n.1417+80_1417+83del
XR_001741157.1:n.1417+80_1417+83del
NM_001178130.3:c.940+80_940+83del	NP_001171601.1:n.940+80_940+83del
NM_001178131.3:c.940+80_940+83del	NP_001171602.1:n.940+80_940+83del
NM_001357021.2:c.940+80_940+83del	NP_001343950.1:n.940+80_940+83del
NM_001963.6:c.940+80_940+83del MANE Select	NP_001954.2:n.940+80_940+83del