Canonical Allele Identifier: CA383238860

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680546A>T (hg19) ; chr11:g.128810651A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810651A>T , CM000673.2:g.128810651A>T	GRCh38
NC_000011.9:g.128680546A>T , CM000673.1:g.128680546A>T	GRCh37
NC_000011.8:g.128185756A>T	NCBI36
NG_032912.1:g.129117A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1043A>T	ENSP00000513017.1:p.Tyr348Phe
ENST00000527786.7:c.1022A>T MANE Select	ENSP00000433488.2:p.Tyr341Phe
ENST00000281428.12:c.824A>T	ENSP00000281428.8:p.Tyr275Phe
ENST00000344954.10:c.443A>T	ENSP00000339627.7:p.Tyr148Phe
ENST00000429175.7:c.*944A>T	ENSP00000399985.3:n.*944A>T
ENST00000527786.6:c.1022A>T	ENSP00000433488.2:p.Tyr341Phe
ENST00000528790.1:n.3605A>T
ENST00000534087.3:c.923A>T	ENSP00000432950.1:p.Tyr308Phe
ENST00000608303.5:c.*414A>T	ENSP00000477262.1:n.*414A>T
NM_001167681.2:c.923A>T	NP_001161153.1:p.Tyr308Phe
NM_001271010.1:c.824A>T	NP_001257939.1:p.Tyr275Phe
NM_001271012.1:c.443A>T	NP_001257941.1:p.Tyr148Phe
NM_002017.4:c.1022A>T	NP_002008.2:p.Tyr341Phe
XM_011542701.1:c.923A>T	XP_011541003.1:p.Tyr308Phe
XM_011542702.1:c.896A>T	XP_011541004.1:p.Tyr299Phe
XM_011542701.2:c.923A>T	XP_011541003.1:p.Tyr308Phe
XM_017017405.1:c.923A>T	XP_016872894.1:p.Tyr308Phe
XM_017017406.1:c.923A>T	XP_016872895.1:p.Tyr308Phe
NM_002017.5:c.1022A>T MANE Select	NP_002008.2:p.Tyr341Phe
NM_001167681.3:c.923A>T	NP_001161153.1:p.Tyr308Phe
NM_001271010.2:c.824A>T	NP_001257939.1:p.Tyr275Phe
NM_001271012.2:c.443A>T	NP_001257941.1:p.Tyr148Phe