Canonical Allele Identifier: CA2008248166

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810487C= , CM000673.2:g.128810487C=	GRCh38
NC_000011.9:g.128680382C= , CM000673.1:g.128680382C=	GRCh37
NC_000011.8:g.128185592C=	NCBI36
NG_032912.1:g.128953C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.879C=	ENSP00000513017.1:p.Phe293=
ENST00000527786.7:c.858C= MANE Select	ENSP00000433488.2:p.Phe286=
ENST00000281428.12:c.660C=	ENSP00000281428.8:p.Phe220=
ENST00000344954.10:c.279C=	ENSP00000339627.7:p.Phe93=
ENST00000429175.7:c.*780C=	ENSP00000399985.3:n.*780C=
ENST00000527786.6:c.858C=	ENSP00000433488.2:p.Phe286=
ENST00000528790.1:n.3441C=
ENST00000534087.3:c.759C=	ENSP00000432950.1:p.Phe253=
ENST00000608303.5:c.*250C=	ENSP00000477262.1:n.*250C=
NM_001167681.2:c.759C=	NP_001161153.1:p.Phe253=
NM_001271010.1:c.660C=	NP_001257939.1:p.Phe220=
NM_001271012.1:c.279C=	NP_001257941.1:p.Phe93=
NM_002017.4:c.858C=	NP_002008.2:p.Phe286=
XM_011542701.1:c.759C=	XP_011541003.1:p.Phe253=
XM_011542702.1:c.732C=	XP_011541004.1:p.Phe244=
XM_011542701.2:c.759C=	XP_011541003.1:p.Phe253=
XM_017017405.1:c.759C=	XP_016872894.1:p.Phe253=
XM_017017406.1:c.759C=	XP_016872895.1:p.Phe253=
NM_002017.5:c.858C= MANE Select	NP_002008.2:p.Phe286=
NM_001167681.3:c.759C=	NP_001161153.1:p.Phe253=
NM_001271010.2:c.660C=	NP_001257939.1:p.Phe220=
NM_001271012.2:c.279C=	NP_001257941.1:p.Phe93=