Canonical Allele Identifier: CA383238479

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680381T>A (hg19) ; chr11:g.128810486T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810486T>A , CM000673.2:g.128810486T>A	GRCh38
NC_000011.9:g.128680381T>A , CM000673.1:g.128680381T>A	GRCh37
NC_000011.8:g.128185591T>A	NCBI36
NG_032912.1:g.128952T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.878T>A	ENSP00000513017.1:p.Phe293Tyr
ENST00000527786.7:c.857T>A MANE Select	ENSP00000433488.2:p.Phe286Tyr
ENST00000281428.12:c.659T>A	ENSP00000281428.8:p.Phe220Tyr
ENST00000344954.10:c.278T>A	ENSP00000339627.7:p.Phe93Tyr
ENST00000429175.7:c.*779T>A	ENSP00000399985.3:n.*779T>A
ENST00000527786.6:c.857T>A	ENSP00000433488.2:p.Phe286Tyr
ENST00000528790.1:n.3440T>A
ENST00000534087.3:c.758T>A	ENSP00000432950.1:p.Phe253Tyr
ENST00000608303.5:c.*249T>A	ENSP00000477262.1:n.*249T>A
NM_001167681.2:c.758T>A	NP_001161153.1:p.Phe253Tyr
NM_001271010.1:c.659T>A	NP_001257939.1:p.Phe220Tyr
NM_001271012.1:c.278T>A	NP_001257941.1:p.Phe93Tyr
NM_002017.4:c.857T>A	NP_002008.2:p.Phe286Tyr
XM_011542701.1:c.758T>A	XP_011541003.1:p.Phe253Tyr
XM_011542702.1:c.731T>A	XP_011541004.1:p.Phe244Tyr
XM_011542701.2:c.758T>A	XP_011541003.1:p.Phe253Tyr
XM_017017405.1:c.758T>A	XP_016872894.1:p.Phe253Tyr
XM_017017406.1:c.758T>A	XP_016872895.1:p.Phe253Tyr
NM_002017.5:c.857T>A MANE Select	NP_002008.2:p.Phe286Tyr
NM_001167681.3:c.758T>A	NP_001161153.1:p.Phe253Tyr
NM_001271010.2:c.659T>A	NP_001257939.1:p.Phe220Tyr
NM_001271012.2:c.278T>A	NP_001257941.1:p.Phe93Tyr