Canonical Allele Identifier: CA2008248294

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810574T= , CM000673.2:g.128810574T=	GRCh38
NC_000011.9:g.128680469T= , CM000673.1:g.128680469T=	GRCh37
NC_000011.8:g.128185679T=	NCBI36
NG_032912.1:g.129040T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.966T=	ENSP00000513017.1:p.Asp322=
ENST00000527786.7:c.945T= MANE Select	ENSP00000433488.2:p.Asp315=
ENST00000281428.12:c.747T=	ENSP00000281428.8:p.Asp249=
ENST00000344954.10:c.366T=	ENSP00000339627.7:p.Asp122=
ENST00000429175.7:c.*867T=	ENSP00000399985.3:n.*867T=
ENST00000527786.6:c.945T=	ENSP00000433488.2:p.Asp315=
ENST00000528790.1:n.3528T=
ENST00000534087.3:c.846T=	ENSP00000432950.1:p.Asp282=
ENST00000608303.5:c.*337T=	ENSP00000477262.1:n.*337T=
NM_001167681.2:c.846T=	NP_001161153.1:p.Asp282=
NM_001271010.1:c.747T=	NP_001257939.1:p.Asp249=
NM_001271012.1:c.366T=	NP_001257941.1:p.Asp122=
NM_002017.4:c.945T=	NP_002008.2:p.Asp315=
XM_011542701.1:c.846T=	XP_011541003.1:p.Asp282=
XM_011542702.1:c.819T=	XP_011541004.1:p.Asp273=
XM_011542701.2:c.846T=	XP_011541003.1:p.Asp282=
XM_017017405.1:c.846T=	XP_016872894.1:p.Asp282=
XM_017017406.1:c.846T=	XP_016872895.1:p.Asp282=
NM_002017.5:c.945T= MANE Select	NP_002008.2:p.Asp315=
NM_001167681.3:c.846T=	NP_001161153.1:p.Asp282=
NM_001271010.2:c.747T=	NP_001257939.1:p.Asp249=
NM_001271012.2:c.366T=	NP_001257941.1:p.Asp122=