Canonical Allele Identifier: CA2008248304

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810587C= , CM000673.2:g.128810587C=	GRCh38
NC_000011.9:g.128680482C= , CM000673.1:g.128680482C=	GRCh37
NC_000011.8:g.128185692C=	NCBI36
NG_032912.1:g.129053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.979C=	ENSP00000513017.1:p.Arg327=
ENST00000527786.7:c.958C= MANE Select	ENSP00000433488.2:p.Arg320=
ENST00000281428.12:c.760C=	ENSP00000281428.8:p.Arg254=
ENST00000344954.10:c.379C=	ENSP00000339627.7:p.Arg127=
ENST00000429175.7:c.*880C=	ENSP00000399985.3:n.*880C=
ENST00000527786.6:c.958C=	ENSP00000433488.2:p.Arg320=
ENST00000528790.1:n.3541C=
ENST00000534087.3:c.859C=	ENSP00000432950.1:p.Arg287=
ENST00000608303.5:c.*350C=	ENSP00000477262.1:n.*350C=
NM_001167681.2:c.859C=	NP_001161153.1:p.Arg287=
NM_001271010.1:c.760C=	NP_001257939.1:p.Arg254=
NM_001271012.1:c.379C=	NP_001257941.1:p.Arg127=
NM_002017.4:c.958C=	NP_002008.2:p.Arg320=
XM_011542701.1:c.859C=	XP_011541003.1:p.Arg287=
XM_011542702.1:c.832C=	XP_011541004.1:p.Arg278=
XM_011542701.2:c.859C=	XP_011541003.1:p.Arg287=
XM_017017405.1:c.859C=	XP_016872894.1:p.Arg287=
XM_017017406.1:c.859C=	XP_016872895.1:p.Arg287=
NM_002017.5:c.958C= MANE Select	NP_002008.2:p.Arg320=
NM_001167681.3:c.859C=	NP_001161153.1:p.Arg287=
NM_001271010.2:c.760C=	NP_001257939.1:p.Arg254=
NM_001271012.2:c.379C=	NP_001257941.1:p.Arg127=