Canonical Allele Identifier: CA2008248234

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810521A= , CM000673.2:g.128810521A=	GRCh38
NC_000011.9:g.128680416A= , CM000673.1:g.128680416A=	GRCh37
NC_000011.8:g.128185626A=	NCBI36
NG_032912.1:g.128987A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.913A=	ENSP00000513017.1:p.Ser305=
ENST00000527786.7:c.892A= MANE Select	ENSP00000433488.2:p.Ser298=
ENST00000281428.12:c.694A=	ENSP00000281428.8:p.Ser232=
ENST00000344954.10:c.313A=	ENSP00000339627.7:p.Ser105=
ENST00000429175.7:c.*814A=	ENSP00000399985.3:n.*814A=
ENST00000527786.6:c.892A=	ENSP00000433488.2:p.Ser298=
ENST00000528790.1:n.3475A=
ENST00000534087.3:c.793A=	ENSP00000432950.1:p.Ser265=
ENST00000608303.5:c.*284A=	ENSP00000477262.1:n.*284A=
NM_001167681.2:c.793A=	NP_001161153.1:p.Ser265=
NM_001271010.1:c.694A=	NP_001257939.1:p.Ser232=
NM_001271012.1:c.313A=	NP_001257941.1:p.Ser105=
NM_002017.4:c.892A=	NP_002008.2:p.Ser298=
XM_011542701.1:c.793A=	XP_011541003.1:p.Ser265=
XM_011542702.1:c.766A=	XP_011541004.1:p.Ser256=
XM_011542701.2:c.793A=	XP_011541003.1:p.Ser265=
XM_017017405.1:c.793A=	XP_016872894.1:p.Ser265=
XM_017017406.1:c.793A=	XP_016872895.1:p.Ser265=
NM_002017.5:c.892A= MANE Select	NP_002008.2:p.Ser298=
NM_001167681.3:c.793A=	NP_001161153.1:p.Ser265=
NM_001271010.2:c.694A=	NP_001257939.1:p.Ser232=
NM_001271012.2:c.313A=	NP_001257941.1:p.Ser105=