Canonical Allele Identifier: CA2008248151
Gene: FLI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810478G= , CM000673.2:g.128810478G= GRCh38
NC_000011.9:g.128680373G= , CM000673.1:g.128680373G= GRCh37
NC_000011.8:g.128185583G= NCBI36
NG_032912.1:g.128944G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.870G= ENSP00000513017.1:p.Leu290=
ENST00000527786.7:c.849G= MANE Select ENSP00000433488.2:p.Leu283=
ENST00000281428.12:c.651G= ENSP00000281428.8:p.Leu217=
ENST00000344954.10:c.270G= ENSP00000339627.7:p.Leu90=
ENST00000429175.7:c.*771G= ENSP00000399985.3:n.*771G=
ENST00000527786.6:c.849G= ENSP00000433488.2:p.Leu283=
ENST00000528790.1:n.3432G=
ENST00000534087.3:c.750G= ENSP00000432950.1:p.Leu250=
ENST00000608303.5:c.*241G= ENSP00000477262.1:n.*241G=
NM_001167681.2:c.750G= NP_001161153.1:p.Leu250=
NM_001271010.1:c.651G= NP_001257939.1:p.Leu217=
NM_001271012.1:c.270G= NP_001257941.1:p.Leu90=
NM_002017.4:c.849G= NP_002008.2:p.Leu283=
XM_011542701.1:c.750G= XP_011541003.1:p.Leu250=
XM_011542702.1:c.723G= XP_011541004.1:p.Leu241=
XM_011542701.2:c.750G= XP_011541003.1:p.Leu250=
XM_017017405.1:c.750G= XP_016872894.1:p.Leu250=
XM_017017406.1:c.750G= XP_016872895.1:p.Leu250=
NM_002017.5:c.849G= MANE Select NP_002008.2:p.Leu283=
NM_001167681.3:c.750G= NP_001161153.1:p.Leu250=
NM_001271010.2:c.651G= NP_001257939.1:p.Leu217=
NM_001271012.2:c.270G= NP_001257941.1:p.Leu90=