Canonical Allele Identifier: CA383238756

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680502C>A (hg19) ; chr11:g.128810607C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810607C>A , CM000673.2:g.128810607C>A	GRCh38
NC_000011.9:g.128680502C>A , CM000673.1:g.128680502C>A	GRCh37
NC_000011.8:g.128185712C>A	NCBI36
NG_032912.1:g.129073C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.999C>A	ENSP00000513017.1:p.Ser333Arg
ENST00000527786.7:c.978C>A MANE Select	ENSP00000433488.2:p.Ser326Arg
ENST00000281428.12:c.780C>A	ENSP00000281428.8:p.Ser260Arg
ENST00000344954.10:c.399C>A	ENSP00000339627.7:p.Ser133Arg
ENST00000429175.7:c.*900C>A	ENSP00000399985.3:n.*900C>A
ENST00000527786.6:c.978C>A	ENSP00000433488.2:p.Ser326Arg
ENST00000528790.1:n.3561C>A
ENST00000534087.3:c.879C>A	ENSP00000432950.1:p.Ser293Arg
ENST00000608303.5:c.*370C>A	ENSP00000477262.1:n.*370C>A
NM_001167681.2:c.879C>A	NP_001161153.1:p.Ser293Arg
NM_001271010.1:c.780C>A	NP_001257939.1:p.Ser260Arg
NM_001271012.1:c.399C>A	NP_001257941.1:p.Ser133Arg
NM_002017.4:c.978C>A	NP_002008.2:p.Ser326Arg
XM_011542701.1:c.879C>A	XP_011541003.1:p.Ser293Arg
XM_011542702.1:c.852C>A	XP_011541004.1:p.Ser284Arg
XM_011542701.2:c.879C>A	XP_011541003.1:p.Ser293Arg
XM_017017405.1:c.879C>A	XP_016872894.1:p.Ser293Arg
XM_017017406.1:c.879C>A	XP_016872895.1:p.Ser293Arg
NM_002017.5:c.978C>A MANE Select	NP_002008.2:p.Ser326Arg
NM_001167681.3:c.879C>A	NP_001161153.1:p.Ser293Arg
NM_001271010.2:c.780C>A	NP_001257939.1:p.Ser260Arg
NM_001271012.2:c.399C>A	NP_001257941.1:p.Ser133Arg