Canonical Allele Identifier: CA2008248492

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810697T= , CM000673.2:g.128810697T=	GRCh38
NC_000011.9:g.128680592T= , CM000673.1:g.128680592T=	GRCh37
NC_000011.8:g.128185802T=	NCBI36
NG_032912.1:g.129163T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1089T=	ENSP00000513017.1:p.Tyr363=
ENST00000527786.7:c.1068T= MANE Select	ENSP00000433488.2:p.Tyr356=
ENST00000281428.12:c.870T=	ENSP00000281428.8:p.Tyr290=
ENST00000344954.10:c.489T=	ENSP00000339627.7:p.Tyr163=
ENST00000429175.7:c.*990T=	ENSP00000399985.3:n.*990T=
ENST00000527786.6:c.1068T=	ENSP00000433488.2:p.Tyr356=
ENST00000528790.1:n.3651T=
ENST00000534087.3:c.969T=	ENSP00000432950.1:p.Tyr323=
ENST00000608303.5:c.*460T=	ENSP00000477262.1:n.*460T=
NM_001167681.2:c.969T=	NP_001161153.1:p.Tyr323=
NM_001271010.1:c.870T=	NP_001257939.1:p.Tyr290=
NM_001271012.1:c.489T=	NP_001257941.1:p.Tyr163=
NM_002017.4:c.1068T=	NP_002008.2:p.Tyr356=
XM_011542701.1:c.969T=	XP_011541003.1:p.Tyr323=
XM_011542702.1:c.942T=	XP_011541004.1:p.Tyr314=
XM_011542701.2:c.969T=	XP_011541003.1:p.Tyr323=
XM_017017405.1:c.969T=	XP_016872894.1:p.Tyr323=
XM_017017406.1:c.969T=	XP_016872895.1:p.Tyr323=
NM_002017.5:c.1068T= MANE Select	NP_002008.2:p.Tyr356=
NM_001167681.3:c.969T=	NP_001161153.1:p.Tyr323=
NM_001271010.2:c.870T=	NP_001257939.1:p.Tyr290=
NM_001271012.2:c.489T=	NP_001257941.1:p.Tyr163=