Canonical Allele Identifier: CA2008248412

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810640G= , CM000673.2:g.128810640G=	GRCh38
NC_000011.9:g.128680535G= , CM000673.1:g.128680535G=	GRCh37
NC_000011.8:g.128185745G=	NCBI36
NG_032912.1:g.129106G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1032G=	ENSP00000513017.1:p.Arg344=
ENST00000527786.7:c.1011G= MANE Select	ENSP00000433488.2:p.Arg337=
ENST00000281428.12:c.813G=	ENSP00000281428.8:p.Arg271=
ENST00000344954.10:c.432G=	ENSP00000339627.7:p.Arg144=
ENST00000429175.7:c.*933G=	ENSP00000399985.3:n.*933G=
ENST00000527786.6:c.1011G=	ENSP00000433488.2:p.Arg337=
ENST00000528790.1:n.3594G=
ENST00000534087.3:c.912G=	ENSP00000432950.1:p.Arg304=
ENST00000608303.5:c.*403G=	ENSP00000477262.1:n.*403G=
NM_001167681.2:c.912G=	NP_001161153.1:p.Arg304=
NM_001271010.1:c.813G=	NP_001257939.1:p.Arg271=
NM_001271012.1:c.432G=	NP_001257941.1:p.Arg144=
NM_002017.4:c.1011G=	NP_002008.2:p.Arg337=
XM_011542701.1:c.912G=	XP_011541003.1:p.Arg304=
XM_011542702.1:c.885G=	XP_011541004.1:p.Arg295=
XM_011542701.2:c.912G=	XP_011541003.1:p.Arg304=
XM_017017405.1:c.912G=	XP_016872894.1:p.Arg304=
XM_017017406.1:c.912G=	XP_016872895.1:p.Arg304=
NM_002017.5:c.1011G= MANE Select	NP_002008.2:p.Arg337=
NM_001167681.3:c.912G=	NP_001161153.1:p.Arg304=
NM_001271010.2:c.813G=	NP_001257939.1:p.Arg271=
NM_001271012.2:c.432G=	NP_001257941.1:p.Arg144=