Canonical Allele Identifier: CA2671756620

Gene: EGF

Linked Data

• gnomAD v4: 4-110011651-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110011651A>G , CM000666.2:g.110011651A>G	GRCh38
NC_000004.11:g.110932807A>G , CM000666.1:g.110932807A>G	GRCh37
NC_000004.10:g.111152256A>G	NCBI36
NG_011441.1:g.103768A>G
NG_011441.2:g.103768A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265171.10:c.*196A>G MANE Select	ENSP00000265171.5:n.*196A>G
ENST00000652245.1:c.*339A>G	ENSP00000498337.1:n.*339A>G
ENST00000265171.9:c.*196A>G	ENSP00000265171.5:n.*196A>G
ENST00000509793.5:c.*196A>G	ENSP00000424316.1:n.*196A>G
ENST00000509996.1:n.1426A>G
ENST00000540840.1:n.229+343A>G
NM_001178130.1:c.*196A>G	NP_001171601.1:n.*196A>G
NM_001178131.1:c.*196A>G	NP_001171602.1:n.*196A>G
NM_001963.4:c.*196A>G	NP_001954.2:n.*196A>G
XM_005262796.2:c.*196A>G	XP_005262853.1:n.*196A>G
XM_005262797.2:c.*196A>G	XP_005262854.1:n.*196A>G
XM_005262798.2:c.*196A>G	XP_005262855.1:n.*196A>G
XM_005262800.2:c.*339A>G	XP_005262857.1:n.*339A>G
XM_005262801.2:c.*196A>G	XP_005262858.1:n.*196A>G
XM_006714124.2:c.*339A>G	XP_006714187.1:n.*339A>G
XM_011531707.1:c.*196A>G	XP_011530009.1:n.*196A>G
NM_001178130.2:c.*196A>G	NP_001171601.1:n.*196A>G
NM_001178131.2:c.*196A>G	NP_001171602.1:n.*196A>G
NM_001357021.1:c.*339A>G	NP_001343950.1:n.*339A>G
NM_001963.5:c.*196A>G	NP_001954.2:n.*196A>G
XM_017007845.1:c.*196A>G	XP_016863334.1:n.*196A>G
XM_017007846.1:c.*196A>G	XP_016863335.1:n.*196A>G
XM_017007847.1:c.*196A>G	XP_016863336.1:n.*196A>G
XM_017007848.1:c.*196A>G	XP_016863337.1:n.*196A>G
XM_017007849.1:c.*196A>G	XP_016863338.1:n.*196A>G
XM_017007850.1:c.*339A>G	XP_016863339.1:n.*339A>G
XM_017007851.1:c.*339A>G	XP_016863340.1:n.*339A>G
NM_001178130.3:c.*196A>G	NP_001171601.1:n.*196A>G
NM_001178131.3:c.*196A>G	NP_001171602.1:n.*196A>G
NM_001357021.2:c.*339A>G	NP_001343950.1:n.*339A>G
NM_001963.6:c.*196A>G MANE Select	NP_001954.2:n.*196A>G