Canonical Allele Identifier: CA103716501
Gene: EGF HGNC NCBI

Linked Data

dbSNP Id: rs953897471

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110011716T>G , CM000666.2:g.110011716T>G GRCh38
NC_000004.11:g.110932872T>G , CM000666.1:g.110932872T>G GRCh37
NC_000004.10:g.111152321T>G NCBI36
NG_011441.1:g.103833T>G
NG_011441.2:g.103833T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265171.10:c.*261T>G MANE Select ENSP00000265171.5:n.*261T>G
ENST00000652245.1:c.*404T>G ENSP00000498337.1:n.*404T>G
ENST00000265171.9:c.*261T>G ENSP00000265171.5:n.*261T>G
ENST00000509793.5:c.*261T>G ENSP00000424316.1:n.*261T>G
ENST00000540840.1:n.229+408T>G
NM_001178130.1:c.*261T>G NP_001171601.1:n.*261T>G
NM_001178131.1:c.*261T>G NP_001171602.1:n.*261T>G
NM_001963.4:c.*261T>G NP_001954.2:n.*261T>G
XM_005262796.2:c.*261T>G XP_005262853.1:n.*261T>G
XM_005262797.2:c.*261T>G XP_005262854.1:n.*261T>G
XM_005262798.2:c.*261T>G XP_005262855.1:n.*261T>G
XM_005262800.2:c.*404T>G XP_005262857.1:n.*404T>G
XM_005262801.2:c.*261T>G XP_005262858.1:n.*261T>G
XM_006714124.2:c.*404T>G XP_006714187.1:n.*404T>G
XM_011531707.1:c.*261T>G XP_011530009.1:n.*261T>G
NM_001178130.2:c.*261T>G NP_001171601.1:n.*261T>G
NM_001178131.2:c.*261T>G NP_001171602.1:n.*261T>G
NM_001357021.1:c.*404T>G NP_001343950.1:n.*404T>G
NM_001963.5:c.*261T>G NP_001954.2:n.*261T>G
XM_017007845.1:c.*261T>G XP_016863334.1:n.*261T>G
XM_017007846.1:c.*261T>G XP_016863335.1:n.*261T>G
XM_017007847.1:c.*261T>G XP_016863336.1:n.*261T>G
XM_017007848.1:c.*261T>G XP_016863337.1:n.*261T>G
XM_017007849.1:c.*261T>G XP_016863338.1:n.*261T>G
XM_017007850.1:c.*404T>G XP_016863339.1:n.*404T>G
XM_017007851.1:c.*404T>G XP_016863340.1:n.*404T>G
NM_001178130.3:c.*261T>G NP_001171601.1:n.*261T>G
NM_001178131.3:c.*261T>G NP_001171602.1:n.*261T>G
NM_001357021.2:c.*404T>G NP_001343950.1:n.*404T>G
NM_001963.6:c.*261T>G MANE Select NP_001954.2:n.*261T>G