Canonical Allele Identifier: CA230604795

Gene: FLI1

Linked Data

• dbSNP Id: rs369900426
• gnomAD v4: 11-128810496-G-A
• MyVariant Identifiers: chr11:g.128680391G>A (hg19) ; chr11:g.128810496G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810496G>A , CM000673.2:g.128810496G>A	GRCh38
NC_000011.9:g.128680391G>A , CM000673.1:g.128680391G>A	GRCh37
NC_000011.8:g.128185601G>A	NCBI36
NG_032912.1:g.128962G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.888G>A	ENSP00000513017.1:p.Glu296=
ENST00000527786.7:c.867G>A MANE Select	ENSP00000433488.2:p.Glu289=
ENST00000281428.12:c.669G>A	ENSP00000281428.8:p.Glu223=
ENST00000344954.10:c.288G>A	ENSP00000339627.7:p.Glu96=
ENST00000429175.7:c.*789G>A	ENSP00000399985.3:n.*789G>A
ENST00000527786.6:c.867G>A	ENSP00000433488.2:p.Glu289=
ENST00000528790.1:n.3450G>A
ENST00000534087.3:c.768G>A	ENSP00000432950.1:p.Glu256=
ENST00000608303.5:c.*259G>A	ENSP00000477262.1:n.*259G>A
NM_001167681.2:c.768G>A	NP_001161153.1:p.Glu256=
NM_001271010.1:c.669G>A	NP_001257939.1:p.Glu223=
NM_001271012.1:c.288G>A	NP_001257941.1:p.Glu96=
NM_002017.4:c.867G>A	NP_002008.2:p.Glu289=
XM_011542701.1:c.768G>A	XP_011541003.1:p.Glu256=
XM_011542702.1:c.741G>A	XP_011541004.1:p.Glu247=
XM_011542701.2:c.768G>A	XP_011541003.1:p.Glu256=
XM_017017405.1:c.768G>A	XP_016872894.1:p.Glu256=
XM_017017406.1:c.768G>A	XP_016872895.1:p.Glu256=
NM_002017.5:c.867G>A MANE Select	NP_002008.2:p.Glu289=
NM_001167681.3:c.768G>A	NP_001161153.1:p.Glu256=
NM_001271010.2:c.669G>A	NP_001257939.1:p.Glu223=
NM_001271012.2:c.288G>A	NP_001257941.1:p.Glu96=