Canonical Allele Identifier: CA383239047

Gene: FLI1

Linked Data

• dbSNP Id: rs1297840530
• gnomAD v2: 11-128680624-A-G
• gnomAD v4: 11-128810729-A-G
• COSMIC: COSM5989745 ; COSM5989746
• MyVariant Identifiers: chr11:g.128680624A>G (hg19) ; chr11:g.128810729A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810729A>G , CM000673.2:g.128810729A>G	GRCh38
NC_000011.9:g.128680624A>G , CM000673.1:g.128680624A>G	GRCh37
NC_000011.8:g.128185834A>G	NCBI36
NG_032912.1:g.129195A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1121A>G	ENSP00000513017.1:p.Gln374Arg
ENST00000527786.7:c.1100A>G MANE Select	ENSP00000433488.2:p.Gln367Arg
ENST00000281428.12:c.902A>G	ENSP00000281428.8:p.Gln301Arg
ENST00000344954.10:c.521A>G	ENSP00000339627.7:p.Gln174Arg
ENST00000429175.7:c.*1022A>G	ENSP00000399985.3:n.*1022A>G
ENST00000527786.6:c.1100A>G	ENSP00000433488.2:p.Gln367Arg
ENST00000528790.1:n.3683A>G
ENST00000534087.3:c.1001A>G	ENSP00000432950.1:p.Gln334Arg
ENST00000608303.5:c.*492A>G	ENSP00000477262.1:n.*492A>G
NM_001167681.2:c.1001A>G	NP_001161153.1:p.Gln334Arg
NM_001271010.1:c.902A>G	NP_001257939.1:p.Gln301Arg
NM_001271012.1:c.521A>G	NP_001257941.1:p.Gln174Arg
NM_002017.4:c.1100A>G	NP_002008.2:p.Gln367Arg
XM_011542701.1:c.1001A>G	XP_011541003.1:p.Gln334Arg
XM_011542702.1:c.974A>G	XP_011541004.1:p.Gln325Arg
XM_011542701.2:c.1001A>G	XP_011541003.1:p.Gln334Arg
XM_017017405.1:c.1001A>G	XP_016872894.1:p.Gln334Arg
XM_017017406.1:c.1001A>G	XP_016872895.1:p.Gln334Arg
NM_002017.5:c.1100A>G MANE Select	NP_002008.2:p.Gln367Arg
NM_001167681.3:c.1001A>G	NP_001161153.1:p.Gln334Arg
NM_001271010.2:c.902A>G	NP_001257939.1:p.Gln301Arg
NM_001271012.2:c.521A>G	NP_001257941.1:p.Gln174Arg