Canonical Allele Identifier: CA2008248218

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810512G= , CM000673.2:g.128810512G=	GRCh38
NC_000011.9:g.128680407G= , CM000673.1:g.128680407G=	GRCh37
NC_000011.8:g.128185617G=	NCBI36
NG_032912.1:g.128978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.904G=	ENSP00000513017.1:p.Ala302=
ENST00000527786.7:c.883G= MANE Select	ENSP00000433488.2:p.Ala295=
ENST00000281428.12:c.685G=	ENSP00000281428.8:p.Ala229=
ENST00000344954.10:c.304G=	ENSP00000339627.7:p.Ala102=
ENST00000429175.7:c.*805G=	ENSP00000399985.3:n.*805G=
ENST00000527786.6:c.883G=	ENSP00000433488.2:p.Ala295=
ENST00000528790.1:n.3466G=
ENST00000534087.3:c.784G=	ENSP00000432950.1:p.Ala262=
ENST00000608303.5:c.*275G=	ENSP00000477262.1:n.*275G=
NM_001167681.2:c.784G=	NP_001161153.1:p.Ala262=
NM_001271010.1:c.685G=	NP_001257939.1:p.Ala229=
NM_001271012.1:c.304G=	NP_001257941.1:p.Ala102=
NM_002017.4:c.883G=	NP_002008.2:p.Ala295=
XM_011542701.1:c.784G=	XP_011541003.1:p.Ala262=
XM_011542702.1:c.757G=	XP_011541004.1:p.Ala253=
XM_011542701.2:c.784G=	XP_011541003.1:p.Ala262=
XM_017017405.1:c.784G=	XP_016872894.1:p.Ala262=
XM_017017406.1:c.784G=	XP_016872895.1:p.Ala262=
NM_002017.5:c.883G= MANE Select	NP_002008.2:p.Ala295=
NM_001167681.3:c.784G=	NP_001161153.1:p.Ala262=
NM_001271010.2:c.685G=	NP_001257939.1:p.Ala229=
NM_001271012.2:c.304G=	NP_001257941.1:p.Ala102=