Canonical Allele Identifier: CA383238500

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680390A>T (hg19) ; chr11:g.128810495A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810495A>T , CM000673.2:g.128810495A>T	GRCh38
NC_000011.9:g.128680390A>T , CM000673.1:g.128680390A>T	GRCh37
NC_000011.8:g.128185600A>T	NCBI36
NG_032912.1:g.128961A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.887A>T	ENSP00000513017.1:p.Glu296Val
ENST00000527786.7:c.866A>T MANE Select	ENSP00000433488.2:p.Glu289Val
ENST00000281428.12:c.668A>T	ENSP00000281428.8:p.Glu223Val
ENST00000344954.10:c.287A>T	ENSP00000339627.7:p.Glu96Val
ENST00000429175.7:c.*788A>T	ENSP00000399985.3:n.*788A>T
ENST00000527786.6:c.866A>T	ENSP00000433488.2:p.Glu289Val
ENST00000528790.1:n.3449A>T
ENST00000534087.3:c.767A>T	ENSP00000432950.1:p.Glu256Val
ENST00000608303.5:c.*258A>T	ENSP00000477262.1:n.*258A>T
NM_001167681.2:c.767A>T	NP_001161153.1:p.Glu256Val
NM_001271010.1:c.668A>T	NP_001257939.1:p.Glu223Val
NM_001271012.1:c.287A>T	NP_001257941.1:p.Glu96Val
NM_002017.4:c.866A>T	NP_002008.2:p.Glu289Val
XM_011542701.1:c.767A>T	XP_011541003.1:p.Glu256Val
XM_011542702.1:c.740A>T	XP_011541004.1:p.Glu247Val
XM_011542701.2:c.767A>T	XP_011541003.1:p.Glu256Val
XM_017017405.1:c.767A>T	XP_016872894.1:p.Glu256Val
XM_017017406.1:c.767A>T	XP_016872895.1:p.Glu256Val
NM_002017.5:c.866A>T MANE Select	NP_002008.2:p.Glu289Val
NM_001167681.3:c.767A>T	NP_001161153.1:p.Glu256Val
NM_001271010.2:c.668A>T	NP_001257939.1:p.Glu223Val
NM_001271012.2:c.287A>T	NP_001257941.1:p.Glu96Val