Canonical Allele Identifier: CA2008248256

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810547C= , CM000673.2:g.128810547C=	GRCh38
NC_000011.9:g.128680442C= , CM000673.1:g.128680442C=	GRCh37
NC_000011.8:g.128185652C=	NCBI36
NG_032912.1:g.129013C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.939C=	ENSP00000513017.1:p.Asn313=
ENST00000527786.7:c.918C= MANE Select	ENSP00000433488.2:p.Asn306=
ENST00000281428.12:c.720C=	ENSP00000281428.8:p.Asn240=
ENST00000344954.10:c.339C=	ENSP00000339627.7:p.Asn113=
ENST00000429175.7:c.*840C=	ENSP00000399985.3:n.*840C=
ENST00000527786.6:c.918C=	ENSP00000433488.2:p.Asn306=
ENST00000528790.1:n.3501C=
ENST00000534087.3:c.819C=	ENSP00000432950.1:p.Asn273=
ENST00000608303.5:c.*310C=	ENSP00000477262.1:n.*310C=
NM_001167681.2:c.819C=	NP_001161153.1:p.Asn273=
NM_001271010.1:c.720C=	NP_001257939.1:p.Asn240=
NM_001271012.1:c.339C=	NP_001257941.1:p.Asn113=
NM_002017.4:c.918C=	NP_002008.2:p.Asn306=
XM_011542701.1:c.819C=	XP_011541003.1:p.Asn273=
XM_011542702.1:c.792C=	XP_011541004.1:p.Asn264=
XM_011542701.2:c.819C=	XP_011541003.1:p.Asn273=
XM_017017405.1:c.819C=	XP_016872894.1:p.Asn273=
XM_017017406.1:c.819C=	XP_016872895.1:p.Asn273=
NM_002017.5:c.918C= MANE Select	NP_002008.2:p.Asn306=
NM_001167681.3:c.819C=	NP_001161153.1:p.Asn273=
NM_001271010.2:c.720C=	NP_001257939.1:p.Asn240=
NM_001271012.2:c.339C=	NP_001257941.1:p.Asn113=