Canonical Allele Identifier: CA2008248273

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810565G= , CM000673.2:g.128810565G=	GRCh38
NC_000011.9:g.128680460G= , CM000673.1:g.128680460G=	GRCh37
NC_000011.8:g.128185670G=	NCBI36
NG_032912.1:g.129031G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.957G=	ENSP00000513017.1:p.Thr319=
ENST00000527786.7:c.936G= MANE Select	ENSP00000433488.2:p.Thr312=
ENST00000281428.12:c.738G=	ENSP00000281428.8:p.Thr246=
ENST00000344954.10:c.357G=	ENSP00000339627.7:p.Thr119=
ENST00000429175.7:c.*858G=	ENSP00000399985.3:n.*858G=
ENST00000527786.6:c.936G=	ENSP00000433488.2:p.Thr312=
ENST00000528790.1:n.3519G=
ENST00000534087.3:c.837G=	ENSP00000432950.1:p.Thr279=
ENST00000608303.5:c.*328G=	ENSP00000477262.1:n.*328G=
NM_001167681.2:c.837G=	NP_001161153.1:p.Thr279=
NM_001271010.1:c.738G=	NP_001257939.1:p.Thr246=
NM_001271012.1:c.357G=	NP_001257941.1:p.Thr119=
NM_002017.4:c.936G=	NP_002008.2:p.Thr312=
XM_011542701.1:c.837G=	XP_011541003.1:p.Thr279=
XM_011542702.1:c.810G=	XP_011541004.1:p.Thr270=
XM_011542701.2:c.837G=	XP_011541003.1:p.Thr279=
XM_017017405.1:c.837G=	XP_016872894.1:p.Thr279=
XM_017017406.1:c.837G=	XP_016872895.1:p.Thr279=
NM_002017.5:c.936G= MANE Select	NP_002008.2:p.Thr312=
NM_001167681.3:c.837G=	NP_001161153.1:p.Thr279=
NM_001271010.2:c.738G=	NP_001257939.1:p.Thr246=
NM_001271012.2:c.357G=	NP_001257941.1:p.Thr119=