Canonical Allele Identifier: CA383238858
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000696982.1:c.1043A>C ENSP00000513017.1:p.Tyr348Ser
ENST00000527786.7:c.1022A>C MANE Select ENSP00000433488.2:p.Tyr341Ser
ENST00000281428.12:c.824A>C ENSP00000281428.8:p.Tyr275Ser
ENST00000344954.10:c.443A>C ENSP00000339627.7:p.Tyr148Ser
ENST00000429175.7:c.*944A>C ENSP00000399985.3:n.*944A>C
ENST00000527786.6:c.1022A>C ENSP00000433488.2:p.Tyr341Ser
ENST00000528790.1:n.3605A>C
ENST00000534087.3:c.923A>C ENSP00000432950.1:p.Tyr308Ser
ENST00000608303.5:c.*414A>C ENSP00000477262.1:n.*414A>C
NM_001167681.2:c.923A>C NP_001161153.1:p.Tyr308Ser
NM_001271010.1:c.824A>C NP_001257939.1:p.Tyr275Ser
NM_001271012.1:c.443A>C NP_001257941.1:p.Tyr148Ser
NM_002017.4:c.1022A>C NP_002008.2:p.Tyr341Ser
XM_011542701.1:c.923A>C XP_011541003.1:p.Tyr308Ser
XM_011542702.1:c.896A>C XP_011541004.1:p.Tyr299Ser
XM_011542701.2:c.923A>C XP_011541003.1:p.Tyr308Ser
XM_017017405.1:c.923A>C XP_016872894.1:p.Tyr308Ser
XM_017017406.1:c.923A>C XP_016872895.1:p.Tyr308Ser
NM_002017.5:c.1022A>C MANE Select NP_002008.2:p.Tyr341Ser
NM_001167681.3:c.923A>C NP_001161153.1:p.Tyr308Ser
NM_001271010.2:c.824A>C NP_001257939.1:p.Tyr275Ser
NM_001271012.2:c.443A>C NP_001257941.1:p.Tyr148Ser