Canonical Allele Identifier: CA383239098
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810753A>C , CM000673.2:g.128810753A>C GRCh38
NC_000011.9:g.128680648A>C , CM000673.1:g.128680648A>C GRCh37
NC_000011.8:g.128185858A>C NCBI36
NG_032912.1:g.129219A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1145A>C ENSP00000513017.1:p.Glu382Ala
ENST00000527786.7:c.1124A>C MANE Select ENSP00000433488.2:p.Glu375Ala
ENST00000281428.12:c.926A>C ENSP00000281428.8:p.Glu309Ala
ENST00000344954.10:c.545A>C ENSP00000339627.7:p.Glu182Ala
ENST00000429175.7:c.*1046A>C ENSP00000399985.3:n.*1046A>C
ENST00000527786.6:c.1124A>C ENSP00000433488.2:p.Glu375Ala
ENST00000528790.1:n.3707A>C
ENST00000534087.3:c.1025A>C ENSP00000432950.1:p.Glu342Ala
ENST00000608303.5:c.*516A>C ENSP00000477262.1:n.*516A>C
NM_001167681.2:c.1025A>C NP_001161153.1:p.Glu342Ala
NM_001271010.1:c.926A>C NP_001257939.1:p.Glu309Ala
NM_001271012.1:c.545A>C NP_001257941.1:p.Glu182Ala
NM_002017.4:c.1124A>C NP_002008.2:p.Glu375Ala
XM_011542701.1:c.1025A>C XP_011541003.1:p.Glu342Ala
XM_011542702.1:c.998A>C XP_011541004.1:p.Glu333Ala
XM_011542701.2:c.1025A>C XP_011541003.1:p.Glu342Ala
XM_017017405.1:c.1025A>C XP_016872894.1:p.Glu342Ala
XM_017017406.1:c.1025A>C XP_016872895.1:p.Glu342Ala
NM_002017.5:c.1124A>C MANE Select NP_002008.2:p.Glu375Ala
NM_001167681.3:c.1025A>C NP_001161153.1:p.Glu342Ala
NM_001271010.2:c.926A>C NP_001257939.1:p.Glu309Ala
NM_001271012.2:c.545A>C NP_001257941.1:p.Glu182Ala