Canonical Allele Identifier: CA477702652

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680631G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810736G>A , CM000673.2:g.128810736G>A	GRCh38
NC_000011.9:g.128680631G>A , CM000673.1:g.128680631G>A	GRCh37
NC_000011.8:g.128185841G>A	NCBI36
NG_032912.1:g.129202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1128G>A	ENSP00000513017.1:p.Leu376=
ENST00000527786.7:c.1107G>A MANE Select	ENSP00000433488.2:p.Leu369=
ENST00000281428.12:c.909G>A	ENSP00000281428.8:p.Leu303=
ENST00000344954.10:c.528G>A	ENSP00000339627.7:p.Leu176=
ENST00000429175.7:c.*1029G>A	ENSP00000399985.3:n.*1029G>A
ENST00000527786.6:c.1107G>A	ENSP00000433488.2:p.Leu369=
ENST00000528790.1:n.3690G>A
ENST00000534087.3:c.1008G>A	ENSP00000432950.1:p.Leu336=
ENST00000608303.5:c.*499G>A	ENSP00000477262.1:n.*499G>A
NM_001167681.2:c.1008G>A	NP_001161153.1:p.Leu336=
NM_001271010.1:c.909G>A	NP_001257939.1:p.Leu303=
NM_001271012.1:c.528G>A	NP_001257941.1:p.Leu176=
NM_002017.4:c.1107G>A	NP_002008.2:p.Leu369=
XM_011542701.1:c.1008G>A	XP_011541003.1:p.Leu336=
XM_011542702.1:c.981G>A	XP_011541004.1:p.Leu327=
XM_011542701.2:c.1008G>A	XP_011541003.1:p.Leu336=
XM_017017405.1:c.1008G>A	XP_016872894.1:p.Leu336=
XM_017017406.1:c.1008G>A	XP_016872895.1:p.Leu336=
NM_002017.5:c.1107G>A MANE Select	NP_002008.2:p.Leu369=
NM_001167681.3:c.1008G>A	NP_001161153.1:p.Leu336=
NM_001271010.2:c.909G>A	NP_001257939.1:p.Leu303=
NM_001271012.2:c.528G>A	NP_001257941.1:p.Leu176=