Canonical Allele Identifier: CA2008248252

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810541G= , CM000673.2:g.128810541G=	GRCh38
NC_000011.9:g.128680436G= , CM000673.1:g.128680436G=	GRCh37
NC_000011.8:g.128185646G=	NCBI36
NG_032912.1:g.129007G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.933G=	ENSP00000513017.1:p.Gly311=
ENST00000527786.7:c.912G= MANE Select	ENSP00000433488.2:p.Gly304=
ENST00000281428.12:c.714G=	ENSP00000281428.8:p.Gly238=
ENST00000344954.10:c.333G=	ENSP00000339627.7:p.Gly111=
ENST00000429175.7:c.*834G=	ENSP00000399985.3:n.*834G=
ENST00000527786.6:c.912G=	ENSP00000433488.2:p.Gly304=
ENST00000528790.1:n.3495G=
ENST00000534087.3:c.813G=	ENSP00000432950.1:p.Gly271=
ENST00000608303.5:c.*304G=	ENSP00000477262.1:n.*304G=
NM_001167681.2:c.813G=	NP_001161153.1:p.Gly271=
NM_001271010.1:c.714G=	NP_001257939.1:p.Gly238=
NM_001271012.1:c.333G=	NP_001257941.1:p.Gly111=
NM_002017.4:c.912G=	NP_002008.2:p.Gly304=
XM_011542701.1:c.813G=	XP_011541003.1:p.Gly271=
XM_011542702.1:c.786G=	XP_011541004.1:p.Gly262=
XM_011542701.2:c.813G=	XP_011541003.1:p.Gly271=
XM_017017405.1:c.813G=	XP_016872894.1:p.Gly271=
XM_017017406.1:c.813G=	XP_016872895.1:p.Gly271=
NM_002017.5:c.912G= MANE Select	NP_002008.2:p.Gly304=
NM_001167681.3:c.813G=	NP_001161153.1:p.Gly271=
NM_001271010.2:c.714G=	NP_001257939.1:p.Gly238=
NM_001271012.2:c.333G=	NP_001257941.1:p.Gly111=