Canonical Allele Identifier: CA2008248202

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810506G= , CM000673.2:g.128810506G=	GRCh38
NC_000011.9:g.128680401G= , CM000673.1:g.128680401G=	GRCh37
NC_000011.8:g.128185611G=	NCBI36
NG_032912.1:g.128972G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.898G=	ENSP00000513017.1:p.Asp300=
ENST00000527786.7:c.877G= MANE Select	ENSP00000433488.2:p.Asp293=
ENST00000281428.12:c.679G=	ENSP00000281428.8:p.Asp227=
ENST00000344954.10:c.298G=	ENSP00000339627.7:p.Asp100=
ENST00000429175.7:c.*799G=	ENSP00000399985.3:n.*799G=
ENST00000527786.6:c.877G=	ENSP00000433488.2:p.Asp293=
ENST00000528790.1:n.3460G=
ENST00000534087.3:c.778G=	ENSP00000432950.1:p.Asp260=
ENST00000608303.5:c.*269G=	ENSP00000477262.1:n.*269G=
NM_001167681.2:c.778G=	NP_001161153.1:p.Asp260=
NM_001271010.1:c.679G=	NP_001257939.1:p.Asp227=
NM_001271012.1:c.298G=	NP_001257941.1:p.Asp100=
NM_002017.4:c.877G=	NP_002008.2:p.Asp293=
XM_011542701.1:c.778G=	XP_011541003.1:p.Asp260=
XM_011542702.1:c.751G=	XP_011541004.1:p.Asp251=
XM_011542701.2:c.778G=	XP_011541003.1:p.Asp260=
XM_017017405.1:c.778G=	XP_016872894.1:p.Asp260=
XM_017017406.1:c.778G=	XP_016872895.1:p.Asp260=
NM_002017.5:c.877G= MANE Select	NP_002008.2:p.Asp293=
NM_001167681.3:c.778G=	NP_001161153.1:p.Asp260=
NM_001271010.2:c.679G=	NP_001257939.1:p.Asp227=
NM_001271012.2:c.298G=	NP_001257941.1:p.Asp100=