Canonical Allele Identifier: CA2008248537

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810748G= , CM000673.2:g.128810748G=	GRCh38
NC_000011.9:g.128680643G= , CM000673.1:g.128680643G=	GRCh37
NC_000011.8:g.128185853G=	NCBI36
NG_032912.1:g.129214G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1140G=	ENSP00000513017.1:p.Pro380=
ENST00000527786.7:c.1119G= MANE Select	ENSP00000433488.2:p.Pro373=
ENST00000281428.12:c.921G=	ENSP00000281428.8:p.Pro307=
ENST00000344954.10:c.540G=	ENSP00000339627.7:p.Pro180=
ENST00000429175.7:c.*1041G=	ENSP00000399985.3:n.*1041G=
ENST00000527786.6:c.1119G=	ENSP00000433488.2:p.Pro373=
ENST00000528790.1:n.3702G=
ENST00000534087.3:c.1020G=	ENSP00000432950.1:p.Pro340=
ENST00000608303.5:c.*511G=	ENSP00000477262.1:n.*511G=
NM_001167681.2:c.1020G=	NP_001161153.1:p.Pro340=
NM_001271010.1:c.921G=	NP_001257939.1:p.Pro307=
NM_001271012.1:c.540G=	NP_001257941.1:p.Pro180=
NM_002017.4:c.1119G=	NP_002008.2:p.Pro373=
XM_011542701.1:c.1020G=	XP_011541003.1:p.Pro340=
XM_011542702.1:c.993G=	XP_011541004.1:p.Pro331=
XM_011542701.2:c.1020G=	XP_011541003.1:p.Pro340=
XM_017017405.1:c.1020G=	XP_016872894.1:p.Pro340=
XM_017017406.1:c.1020G=	XP_016872895.1:p.Pro340=
NM_002017.5:c.1119G= MANE Select	NP_002008.2:p.Pro373=
NM_001167681.3:c.1020G=	NP_001161153.1:p.Pro340=
NM_001271010.2:c.921G=	NP_001257939.1:p.Pro307=
NM_001271012.2:c.540G=	NP_001257941.1:p.Pro180=