Canonical Allele Identifier: CA383239044
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810728C>G , CM000673.2:g.128810728C>G GRCh38
NC_000011.9:g.128680623C>G , CM000673.1:g.128680623C>G GRCh37
NC_000011.8:g.128185833C>G NCBI36
NG_032912.1:g.129194C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1120C>G ENSP00000513017.1:p.Gln374Glu
ENST00000527786.7:c.1099C>G MANE Select ENSP00000433488.2:p.Gln367Glu
ENST00000281428.12:c.901C>G ENSP00000281428.8:p.Gln301Glu
ENST00000344954.10:c.520C>G ENSP00000339627.7:p.Gln174Glu
ENST00000429175.7:c.*1021C>G ENSP00000399985.3:n.*1021C>G
ENST00000527786.6:c.1099C>G ENSP00000433488.2:p.Gln367Glu
ENST00000528790.1:n.3682C>G
ENST00000534087.3:c.1000C>G ENSP00000432950.1:p.Gln334Glu
ENST00000608303.5:c.*491C>G ENSP00000477262.1:n.*491C>G
NM_001167681.2:c.1000C>G NP_001161153.1:p.Gln334Glu
NM_001271010.1:c.901C>G NP_001257939.1:p.Gln301Glu
NM_001271012.1:c.520C>G NP_001257941.1:p.Gln174Glu
NM_002017.4:c.1099C>G NP_002008.2:p.Gln367Glu
XM_011542701.1:c.1000C>G XP_011541003.1:p.Gln334Glu
XM_011542702.1:c.973C>G XP_011541004.1:p.Gln325Glu
XM_011542701.2:c.1000C>G XP_011541003.1:p.Gln334Glu
XM_017017405.1:c.1000C>G XP_016872894.1:p.Gln334Glu
XM_017017406.1:c.1000C>G XP_016872895.1:p.Gln334Glu
NM_002017.5:c.1099C>G MANE Select NP_002008.2:p.Gln367Glu
NM_001167681.3:c.1000C>G NP_001161153.1:p.Gln334Glu
NM_001271010.2:c.901C>G NP_001257939.1:p.Gln301Glu
NM_001271012.2:c.520C>G NP_001257941.1:p.Gln174Glu