Canonical Allele Identifier: CA2008248558
Gene: FLI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810759C= , CM000673.2:g.128810759C= GRCh38
NC_000011.9:g.128680654C= , CM000673.1:g.128680654C= GRCh37
NC_000011.8:g.128185864C= NCBI36
NG_032912.1:g.129225C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1151C= ENSP00000513017.1:p.Ser384=
ENST00000527786.7:c.1130C= MANE Select ENSP00000433488.2:p.Ser377=
ENST00000281428.12:c.932C= ENSP00000281428.8:p.Ser311=
ENST00000344954.10:c.551C= ENSP00000339627.7:p.Ser184=
ENST00000429175.7:c.*1052C= ENSP00000399985.3:n.*1052C=
ENST00000527786.6:c.1130C= ENSP00000433488.2:p.Ser377=
ENST00000528790.1:n.3713C=
ENST00000534087.3:c.1031C= ENSP00000432950.1:p.Ser344=
ENST00000608303.5:c.*522C= ENSP00000477262.1:n.*522C=
NM_001167681.2:c.1031C= NP_001161153.1:p.Ser344=
NM_001271010.1:c.932C= NP_001257939.1:p.Ser311=
NM_001271012.1:c.551C= NP_001257941.1:p.Ser184=
NM_002017.4:c.1130C= NP_002008.2:p.Ser377=
XM_011542701.1:c.1031C= XP_011541003.1:p.Ser344=
XM_011542702.1:c.1004C= XP_011541004.1:p.Ser335=
XM_011542701.2:c.1031C= XP_011541003.1:p.Ser344=
XM_017017405.1:c.1031C= XP_016872894.1:p.Ser344=
XM_017017406.1:c.1031C= XP_016872895.1:p.Ser344=
NM_002017.5:c.1130C= MANE Select NP_002008.2:p.Ser377=
NM_001167681.3:c.1031C= NP_001161153.1:p.Ser344=
NM_001271010.2:c.932C= NP_001257939.1:p.Ser311=
NM_001271012.2:c.551C= NP_001257941.1:p.Ser184=