Canonical Allele Identifier: CA2008248393

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810634G= , CM000673.2:g.128810634G=	GRCh38
NC_000011.9:g.128680529G= , CM000673.1:g.128680529G=	GRCh37
NC_000011.8:g.128185739G=	NCBI36
NG_032912.1:g.129100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1026G=	ENSP00000513017.1:p.Leu342=
ENST00000527786.7:c.1005G= MANE Select	ENSP00000433488.2:p.Leu335=
ENST00000281428.12:c.807G=	ENSP00000281428.8:p.Leu269=
ENST00000344954.10:c.426G=	ENSP00000339627.7:p.Leu142=
ENST00000429175.7:c.*927G=	ENSP00000399985.3:n.*927G=
ENST00000527786.6:c.1005G=	ENSP00000433488.2:p.Leu335=
ENST00000528790.1:n.3588G=
ENST00000534087.3:c.906G=	ENSP00000432950.1:p.Leu302=
ENST00000608303.5:c.*397G=	ENSP00000477262.1:n.*397G=
NM_001167681.2:c.906G=	NP_001161153.1:p.Leu302=
NM_001271010.1:c.807G=	NP_001257939.1:p.Leu269=
NM_001271012.1:c.426G=	NP_001257941.1:p.Leu142=
NM_002017.4:c.1005G=	NP_002008.2:p.Leu335=
XM_011542701.1:c.906G=	XP_011541003.1:p.Leu302=
XM_011542702.1:c.879G=	XP_011541004.1:p.Leu293=
XM_011542701.2:c.906G=	XP_011541003.1:p.Leu302=
XM_017017405.1:c.906G=	XP_016872894.1:p.Leu302=
XM_017017406.1:c.906G=	XP_016872895.1:p.Leu302=
NM_002017.5:c.1005G= MANE Select	NP_002008.2:p.Leu335=
NM_001167681.3:c.906G=	NP_001161153.1:p.Leu302=
NM_001271010.2:c.807G=	NP_001257939.1:p.Leu269=
NM_001271012.2:c.426G=	NP_001257941.1:p.Leu142=