Canonical Allele Identifier: CA383238499
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810495A>G , CM000673.2:g.128810495A>G GRCh38
NC_000011.9:g.128680390A>G , CM000673.1:g.128680390A>G GRCh37
NC_000011.8:g.128185600A>G NCBI36
NG_032912.1:g.128961A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.887A>G ENSP00000513017.1:p.Glu296Gly
ENST00000527786.7:c.866A>G MANE Select ENSP00000433488.2:p.Glu289Gly
ENST00000281428.12:c.668A>G ENSP00000281428.8:p.Glu223Gly
ENST00000344954.10:c.287A>G ENSP00000339627.7:p.Glu96Gly
ENST00000429175.7:c.*788A>G ENSP00000399985.3:n.*788A>G
ENST00000527786.6:c.866A>G ENSP00000433488.2:p.Glu289Gly
ENST00000528790.1:n.3449A>G
ENST00000534087.3:c.767A>G ENSP00000432950.1:p.Glu256Gly
ENST00000608303.5:c.*258A>G ENSP00000477262.1:n.*258A>G
NM_001167681.2:c.767A>G NP_001161153.1:p.Glu256Gly
NM_001271010.1:c.668A>G NP_001257939.1:p.Glu223Gly
NM_001271012.1:c.287A>G NP_001257941.1:p.Glu96Gly
NM_002017.4:c.866A>G NP_002008.2:p.Glu289Gly
XM_011542701.1:c.767A>G XP_011541003.1:p.Glu256Gly
XM_011542702.1:c.740A>G XP_011541004.1:p.Glu247Gly
XM_011542701.2:c.767A>G XP_011541003.1:p.Glu256Gly
XM_017017405.1:c.767A>G XP_016872894.1:p.Glu256Gly
XM_017017406.1:c.767A>G XP_016872895.1:p.Glu256Gly
NM_002017.5:c.866A>G MANE Select NP_002008.2:p.Glu289Gly
NM_001167681.3:c.767A>G NP_001161153.1:p.Glu256Gly
NM_001271010.2:c.668A>G NP_001257939.1:p.Glu223Gly
NM_001271012.2:c.287A>G NP_001257941.1:p.Glu96Gly