Canonical Allele Identifier: CA2008248350
Gene: FLI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810605A= , CM000673.2:g.128810605A= GRCh38
NC_000011.9:g.128680500A= , CM000673.1:g.128680500A= GRCh37
NC_000011.8:g.128185710A= NCBI36
NG_032912.1:g.129071A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.997A= ENSP00000513017.1:p.Ser333=
ENST00000527786.7:c.976A= MANE Select ENSP00000433488.2:p.Ser326=
ENST00000281428.12:c.778A= ENSP00000281428.8:p.Ser260=
ENST00000344954.10:c.397A= ENSP00000339627.7:p.Ser133=
ENST00000429175.7:c.*898A= ENSP00000399985.3:n.*898A=
ENST00000527786.6:c.976A= ENSP00000433488.2:p.Ser326=
ENST00000528790.1:n.3559A=
ENST00000534087.3:c.877A= ENSP00000432950.1:p.Ser293=
ENST00000608303.5:c.*368A= ENSP00000477262.1:n.*368A=
NM_001167681.2:c.877A= NP_001161153.1:p.Ser293=
NM_001271010.1:c.778A= NP_001257939.1:p.Ser260=
NM_001271012.1:c.397A= NP_001257941.1:p.Ser133=
NM_002017.4:c.976A= NP_002008.2:p.Ser326=
XM_011542701.1:c.877A= XP_011541003.1:p.Ser293=
XM_011542702.1:c.850A= XP_011541004.1:p.Ser284=
XM_011542701.2:c.877A= XP_011541003.1:p.Ser293=
XM_017017405.1:c.877A= XP_016872894.1:p.Ser293=
XM_017017406.1:c.877A= XP_016872895.1:p.Ser293=
NM_002017.5:c.976A= MANE Select NP_002008.2:p.Ser326=
NM_001167681.3:c.877A= NP_001161153.1:p.Ser293=
NM_001271010.2:c.778A= NP_001257939.1:p.Ser260=
NM_001271012.2:c.397A= NP_001257941.1:p.Ser133=