Canonical Allele Identifier: CA3043512
Gene: EGF HGNC NCBI

Linked Data

dbSNP Id: rs764972836

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109945257G>T , CM000666.2:g.109945257G>T GRCh38
NC_000004.11:g.110866413G>T , CM000666.1:g.110866413G>T GRCh37
NC_000004.10:g.111085862G>T NCBI36
NG_011441.1:g.37374G>T
NG_011441.2:g.37374G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265171.10:c.922G>T MANE Select ENSP00000265171.5:p.Asp308Tyr
ENST00000652245.1:c.922G>T ENSP00000498337.1:p.Asp308Tyr
ENST00000265171.9:c.922G>T ENSP00000265171.5:p.Asp308Tyr
ENST00000503392.1:c.922G>T ENSP00000421384.1:p.Asp308Tyr
ENST00000509793.5:c.922G>T ENSP00000424316.1:p.Asp308Tyr
NM_001178130.1:c.922G>T NP_001171601.1:p.Asp308Tyr
NM_001178131.1:c.922G>T NP_001171602.1:p.Asp308Tyr
NM_001963.4:c.922G>T NP_001954.2:p.Asp308Tyr
XM_005262796.2:c.922G>T XP_005262853.1:p.Asp308Tyr
XM_005262797.2:c.922G>T XP_005262854.1:p.Asp308Tyr
XM_005262798.2:c.922G>T XP_005262855.1:p.Asp308Tyr
XM_005262800.2:c.922G>T XP_005262857.1:p.Asp308Tyr
XM_005262801.2:c.922G>T XP_005262858.1:p.Asp308Tyr
XM_005262802.2:c.922G>T XP_005262859.1:p.Asp308Tyr
XM_006714124.2:c.922G>T XP_006714187.1:p.Asp308Tyr
XM_011531707.1:c.811G>T XP_011530009.1:p.Asp271Tyr
XM_011531708.1:c.922G>T XP_011530010.1:p.Asp308Tyr
XM_011531709.1:c.922G>T XP_011530011.1:p.Asp308Tyr
XR_427532.2:n.1375G>T
XR_938699.1:n.1375G>T
NM_001178130.2:c.922G>T NP_001171601.1:p.Asp308Tyr
NM_001178131.2:c.922G>T NP_001171602.1:p.Asp308Tyr
NM_001357021.1:c.922G>T NP_001343950.1:p.Asp308Tyr
NM_001963.5:c.922G>T NP_001954.2:p.Asp308Tyr
XM_017007845.1:c.946G>T XP_016863334.1:p.Asp316Tyr
XM_017007846.1:c.946G>T XP_016863335.1:p.Asp316Tyr
XM_017007847.1:c.946G>T XP_016863336.1:p.Asp316Tyr
XM_017007848.1:c.946G>T XP_016863337.1:p.Asp316Tyr
XM_017007849.1:c.946G>T XP_016863338.1:p.Asp316Tyr
XM_017007850.1:c.946G>T XP_016863339.1:p.Asp316Tyr
XM_017007851.1:c.946G>T XP_016863340.1:p.Asp316Tyr
XM_017007853.1:c.946G>T XP_016863342.1:p.Asp316Tyr
XM_017007854.1:c.946G>T XP_016863343.1:p.Asp316Tyr
XM_017007855.1:c.946G>T XP_016863344.1:p.Asp316Tyr
XR_001741156.1:n.1399G>T
XR_001741157.1:n.1399G>T
NM_001178130.3:c.922G>T NP_001171601.1:p.Asp308Tyr
NM_001178131.3:c.922G>T NP_001171602.1:p.Asp308Tyr
NM_001357021.2:c.922G>T NP_001343950.1:p.Asp308Tyr
NM_001963.6:c.922G>T MANE Select NP_001954.2:p.Asp308Tyr