Canonical Allele Identifier: CA383238467

Gene: FLI1

Linked Data

• ClinVar Variation Id: 986337
• ClinVar RCV Id: RCV001267651
• dbSNP Id: rs1942909159
• MyVariant Identifiers: chr11:g.128680376G>T (hg19) ; chr11:g.128810481G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810481G>T , CM000673.2:g.128810481G>T	GRCh38
NC_000011.9:g.128680376G>T , CM000673.1:g.128680376G>T	GRCh37
NC_000011.8:g.128185586G>T	NCBI36
NG_032912.1:g.128947G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.873G>T	ENSP00000513017.1:p.Trp291Cys
ENST00000527786.7:c.852G>T MANE Select	ENSP00000433488.2:p.Trp284Cys
ENST00000281428.12:c.654G>T	ENSP00000281428.8:p.Trp218Cys
ENST00000344954.10:c.273G>T	ENSP00000339627.7:p.Trp91Cys
ENST00000429175.7:c.*774G>T	ENSP00000399985.3:n.*774G>T
ENST00000527786.6:c.852G>T	ENSP00000433488.2:p.Trp284Cys
ENST00000528790.1:n.3435G>T
ENST00000534087.3:c.753G>T	ENSP00000432950.1:p.Trp251Cys
ENST00000608303.5:c.*244G>T	ENSP00000477262.1:n.*244G>T
NM_001167681.2:c.753G>T	NP_001161153.1:p.Trp251Cys
NM_001271010.1:c.654G>T	NP_001257939.1:p.Trp218Cys
NM_001271012.1:c.273G>T	NP_001257941.1:p.Trp91Cys
NM_002017.4:c.852G>T	NP_002008.2:p.Trp284Cys
XM_011542701.1:c.753G>T	XP_011541003.1:p.Trp251Cys
XM_011542702.1:c.726G>T	XP_011541004.1:p.Trp242Cys
XM_011542701.2:c.753G>T	XP_011541003.1:p.Trp251Cys
XM_017017405.1:c.753G>T	XP_016872894.1:p.Trp251Cys
XM_017017406.1:c.753G>T	XP_016872895.1:p.Trp251Cys
NM_002017.5:c.852G>T MANE Select	NP_002008.2:p.Trp284Cys
NM_001167681.3:c.753G>T	NP_001161153.1:p.Trp251Cys
NM_001271010.2:c.654G>T	NP_001257939.1:p.Trp218Cys
NM_001271012.2:c.273G>T	NP_001257941.1:p.Trp91Cys