Canonical Allele Identifier: CA2008248489

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810694A= , CM000673.2:g.128810694A=	GRCh38
NC_000011.9:g.128680589A= , CM000673.1:g.128680589A=	GRCh37
NC_000011.8:g.128185799A=	NCBI36
NG_032912.1:g.129160A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1086A=	ENSP00000513017.1:p.Arg362=
ENST00000527786.7:c.1065A= MANE Select	ENSP00000433488.2:p.Arg355=
ENST00000281428.12:c.867A=	ENSP00000281428.8:p.Arg289=
ENST00000344954.10:c.486A=	ENSP00000339627.7:p.Arg162=
ENST00000429175.7:c.*987A=	ENSP00000399985.3:n.*987A=
ENST00000527786.6:c.1065A=	ENSP00000433488.2:p.Arg355=
ENST00000528790.1:n.3648A=
ENST00000534087.3:c.966A=	ENSP00000432950.1:p.Arg322=
ENST00000608303.5:c.*457A=	ENSP00000477262.1:n.*457A=
NM_001167681.2:c.966A=	NP_001161153.1:p.Arg322=
NM_001271010.1:c.867A=	NP_001257939.1:p.Arg289=
NM_001271012.1:c.486A=	NP_001257941.1:p.Arg162=
NM_002017.4:c.1065A=	NP_002008.2:p.Arg355=
XM_011542701.1:c.966A=	XP_011541003.1:p.Arg322=
XM_011542702.1:c.939A=	XP_011541004.1:p.Arg313=
XM_011542701.2:c.966A=	XP_011541003.1:p.Arg322=
XM_017017405.1:c.966A=	XP_016872894.1:p.Arg322=
XM_017017406.1:c.966A=	XP_016872895.1:p.Arg322=
NM_002017.5:c.1065A= MANE Select	NP_002008.2:p.Arg355=
NM_001167681.3:c.966A=	NP_001161153.1:p.Arg322=
NM_001271010.2:c.867A=	NP_001257939.1:p.Arg289=
NM_001271012.2:c.486A=	NP_001257941.1:p.Arg162=