Canonical Allele Identifier: CA383239107
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810756C>G , CM000673.2:g.128810756C>G GRCh38
NC_000011.9:g.128680651C>G , CM000673.1:g.128680651C>G GRCh37
NC_000011.8:g.128185861C>G NCBI36
NG_032912.1:g.129222C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1148C>G ENSP00000513017.1:p.Ser383Trp
ENST00000527786.7:c.1127C>G MANE Select ENSP00000433488.2:p.Ser376Trp
ENST00000281428.12:c.929C>G ENSP00000281428.8:p.Ser310Trp
ENST00000344954.10:c.548C>G ENSP00000339627.7:p.Ser183Trp
ENST00000429175.7:c.*1049C>G ENSP00000399985.3:n.*1049C>G
ENST00000527786.6:c.1127C>G ENSP00000433488.2:p.Ser376Trp
ENST00000528790.1:n.3710C>G
ENST00000534087.3:c.1028C>G ENSP00000432950.1:p.Ser343Trp
ENST00000608303.5:c.*519C>G ENSP00000477262.1:n.*519C>G
NM_001167681.2:c.1028C>G NP_001161153.1:p.Ser343Trp
NM_001271010.1:c.929C>G NP_001257939.1:p.Ser310Trp
NM_001271012.1:c.548C>G NP_001257941.1:p.Ser183Trp
NM_002017.4:c.1127C>G NP_002008.2:p.Ser376Trp
XM_011542701.1:c.1028C>G XP_011541003.1:p.Ser343Trp
XM_011542702.1:c.1001C>G XP_011541004.1:p.Ser334Trp
XM_011542701.2:c.1028C>G XP_011541003.1:p.Ser343Trp
XM_017017405.1:c.1028C>G XP_016872894.1:p.Ser343Trp
XM_017017406.1:c.1028C>G XP_016872895.1:p.Ser343Trp
NM_002017.5:c.1127C>G MANE Select NP_002008.2:p.Ser376Trp
NM_001167681.3:c.1028C>G NP_001161153.1:p.Ser343Trp
NM_001271010.2:c.929C>G NP_001257939.1:p.Ser310Trp
NM_001271012.2:c.548C>G NP_001257941.1:p.Ser183Trp