Canonical Allele Identifier: CA2008248135
Gene: FLI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810462G= , CM000673.2:g.128810462G= GRCh38
NC_000011.9:g.128680357G= , CM000673.1:g.128680357G= GRCh37
NC_000011.8:g.128185567G= NCBI36
NG_032912.1:g.128928G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.854G= ENSP00000513017.1:p.Ser285=
ENST00000527786.7:c.833G= MANE Select ENSP00000433488.2:p.Ser278=
ENST00000281428.12:c.635G= ENSP00000281428.8:p.Ser212=
ENST00000344954.10:c.254G= ENSP00000339627.7:p.Ser85=
ENST00000429175.7:c.*755G= ENSP00000399985.3:n.*755G=
ENST00000527786.6:c.833G= ENSP00000433488.2:p.Ser278=
ENST00000528790.1:n.3416G=
ENST00000534087.3:c.734G= ENSP00000432950.1:p.Ser245=
ENST00000608303.5:c.*225G= ENSP00000477262.1:n.*225G=
NM_001167681.2:c.734G= NP_001161153.1:p.Ser245=
NM_001271010.1:c.635G= NP_001257939.1:p.Ser212=
NM_001271012.1:c.254G= NP_001257941.1:p.Ser85=
NM_002017.4:c.833G= NP_002008.2:p.Ser278=
XM_011542701.1:c.734G= XP_011541003.1:p.Ser245=
XM_011542702.1:c.707G= XP_011541004.1:p.Ser236=
XM_011542701.2:c.734G= XP_011541003.1:p.Ser245=
XM_017017405.1:c.734G= XP_016872894.1:p.Ser245=
XM_017017406.1:c.734G= XP_016872895.1:p.Ser245=
NM_002017.5:c.833G= MANE Select NP_002008.2:p.Ser278=
NM_001167681.3:c.734G= NP_001161153.1:p.Ser245=
NM_001271010.2:c.635G= NP_001257939.1:p.Ser212=
NM_001271012.2:c.254G= NP_001257941.1:p.Ser85=