Canonical Allele Identifier: CA2008248266

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810559A= , CM000673.2:g.128810559A=	GRCh38
NC_000011.9:g.128680454A= , CM000673.1:g.128680454A=	GRCh37
NC_000011.8:g.128185664A=	NCBI36
NG_032912.1:g.129025A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.951A=	ENSP00000513017.1:p.Lys317=
ENST00000527786.7:c.930A= MANE Select	ENSP00000433488.2:p.Lys310=
ENST00000281428.12:c.732A=	ENSP00000281428.8:p.Lys244=
ENST00000344954.10:c.351A=	ENSP00000339627.7:p.Lys117=
ENST00000429175.7:c.*852A=	ENSP00000399985.3:n.*852A=
ENST00000527786.6:c.930A=	ENSP00000433488.2:p.Lys310=
ENST00000528790.1:n.3513A=
ENST00000534087.3:c.831A=	ENSP00000432950.1:p.Lys277=
ENST00000608303.5:c.*322A=	ENSP00000477262.1:n.*322A=
NM_001167681.2:c.831A=	NP_001161153.1:p.Lys277=
NM_001271010.1:c.732A=	NP_001257939.1:p.Lys244=
NM_001271012.1:c.351A=	NP_001257941.1:p.Lys117=
NM_002017.4:c.930A=	NP_002008.2:p.Lys310=
XM_011542701.1:c.831A=	XP_011541003.1:p.Lys277=
XM_011542702.1:c.804A=	XP_011541004.1:p.Lys268=
XM_011542701.2:c.831A=	XP_011541003.1:p.Lys277=
XM_017017405.1:c.831A=	XP_016872894.1:p.Lys277=
XM_017017406.1:c.831A=	XP_016872895.1:p.Lys277=
NM_002017.5:c.930A= MANE Select	NP_002008.2:p.Lys310=
NM_001167681.3:c.831A=	NP_001161153.1:p.Lys277=
NM_001271010.2:c.732A=	NP_001257939.1:p.Lys244=
NM_001271012.2:c.351A=	NP_001257941.1:p.Lys117=