Canonical Allele Identifier: CA2008248254

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810544C= , CM000673.2:g.128810544C=	GRCh38
NC_000011.9:g.128680439C= , CM000673.1:g.128680439C=	GRCh37
NC_000011.8:g.128185649C=	NCBI36
NG_032912.1:g.129010C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.936C=	ENSP00000513017.1:p.Thr312=
ENST00000527786.7:c.915C= MANE Select	ENSP00000433488.2:p.Thr305=
ENST00000281428.12:c.717C=	ENSP00000281428.8:p.Thr239=
ENST00000344954.10:c.336C=	ENSP00000339627.7:p.Thr112=
ENST00000429175.7:c.*837C=	ENSP00000399985.3:n.*837C=
ENST00000527786.6:c.915C=	ENSP00000433488.2:p.Thr305=
ENST00000528790.1:n.3498C=
ENST00000534087.3:c.816C=	ENSP00000432950.1:p.Thr272=
ENST00000608303.5:c.*307C=	ENSP00000477262.1:n.*307C=
NM_001167681.2:c.816C=	NP_001161153.1:p.Thr272=
NM_001271010.1:c.717C=	NP_001257939.1:p.Thr239=
NM_001271012.1:c.336C=	NP_001257941.1:p.Thr112=
NM_002017.4:c.915C=	NP_002008.2:p.Thr305=
XM_011542701.1:c.816C=	XP_011541003.1:p.Thr272=
XM_011542702.1:c.789C=	XP_011541004.1:p.Thr263=
XM_011542701.2:c.816C=	XP_011541003.1:p.Thr272=
XM_017017405.1:c.816C=	XP_016872894.1:p.Thr272=
XM_017017406.1:c.816C=	XP_016872895.1:p.Thr272=
NM_002017.5:c.915C= MANE Select	NP_002008.2:p.Thr305=
NM_001167681.3:c.816C=	NP_001161153.1:p.Thr272=
NM_001271010.2:c.717C=	NP_001257939.1:p.Thr239=
NM_001271012.2:c.336C=	NP_001257941.1:p.Thr112=