Canonical Allele Identifier: CA383238578

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680425A>T (hg19) ; chr11:g.128810530A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810530A>T , CM000673.2:g.128810530A>T	GRCh38
NC_000011.9:g.128680425A>T , CM000673.1:g.128680425A>T	GRCh37
NC_000011.8:g.128185635A>T	NCBI36
NG_032912.1:g.128996A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.922A>T	ENSP00000513017.1:p.Thr308Ser
ENST00000527786.7:c.901A>T MANE Select	ENSP00000433488.2:p.Thr301Ser
ENST00000281428.12:c.703A>T	ENSP00000281428.8:p.Thr235Ser
ENST00000344954.10:c.322A>T	ENSP00000339627.7:p.Thr108Ser
ENST00000429175.7:c.*823A>T	ENSP00000399985.3:n.*823A>T
ENST00000527786.6:c.901A>T	ENSP00000433488.2:p.Thr301Ser
ENST00000528790.1:n.3484A>T
ENST00000534087.3:c.802A>T	ENSP00000432950.1:p.Thr268Ser
ENST00000608303.5:c.*293A>T	ENSP00000477262.1:n.*293A>T
NM_001167681.2:c.802A>T	NP_001161153.1:p.Thr268Ser
NM_001271010.1:c.703A>T	NP_001257939.1:p.Thr235Ser
NM_001271012.1:c.322A>T	NP_001257941.1:p.Thr108Ser
NM_002017.4:c.901A>T	NP_002008.2:p.Thr301Ser
XM_011542701.1:c.802A>T	XP_011541003.1:p.Thr268Ser
XM_011542702.1:c.775A>T	XP_011541004.1:p.Thr259Ser
XM_011542701.2:c.802A>T	XP_011541003.1:p.Thr268Ser
XM_017017405.1:c.802A>T	XP_016872894.1:p.Thr268Ser
XM_017017406.1:c.802A>T	XP_016872895.1:p.Thr268Ser
NM_002017.5:c.901A>T MANE Select	NP_002008.2:p.Thr301Ser
NM_001167681.3:c.802A>T	NP_001161153.1:p.Thr268Ser
NM_001271010.2:c.703A>T	NP_001257939.1:p.Thr235Ser
NM_001271012.2:c.322A>T	NP_001257941.1:p.Thr108Ser