Canonical Allele Identifier: CA2008248335

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810599C= , CM000673.2:g.128810599C=	GRCh38
NC_000011.9:g.128680494C= , CM000673.1:g.128680494C=	GRCh37
NC_000011.8:g.128185704C=	NCBI36
NG_032912.1:g.129065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.991C=	ENSP00000513017.1:p.Arg331=
ENST00000527786.7:c.970C= MANE Select	ENSP00000433488.2:p.Arg324=
ENST00000281428.12:c.772C=	ENSP00000281428.8:p.Arg258=
ENST00000344954.10:c.391C=	ENSP00000339627.7:p.Arg131=
ENST00000429175.7:c.*892C=	ENSP00000399985.3:n.*892C=
ENST00000527786.6:c.970C=	ENSP00000433488.2:p.Arg324=
ENST00000528790.1:n.3553C=
ENST00000534087.3:c.871C=	ENSP00000432950.1:p.Arg291=
ENST00000608303.5:c.*362C=	ENSP00000477262.1:n.*362C=
NM_001167681.2:c.871C=	NP_001161153.1:p.Arg291=
NM_001271010.1:c.772C=	NP_001257939.1:p.Arg258=
NM_001271012.1:c.391C=	NP_001257941.1:p.Arg131=
NM_002017.4:c.970C=	NP_002008.2:p.Arg324=
XM_011542701.1:c.871C=	XP_011541003.1:p.Arg291=
XM_011542702.1:c.844C=	XP_011541004.1:p.Arg282=
XM_011542701.2:c.871C=	XP_011541003.1:p.Arg291=
XM_017017405.1:c.871C=	XP_016872894.1:p.Arg291=
XM_017017406.1:c.871C=	XP_016872895.1:p.Arg291=
NM_002017.5:c.970C= MANE Select	NP_002008.2:p.Arg324=
NM_001167681.3:c.871C=	NP_001161153.1:p.Arg291=
NM_001271010.2:c.772C=	NP_001257939.1:p.Arg258=
NM_001271012.2:c.391C=	NP_001257941.1:p.Arg131=