Canonical Allele Identifier: CA383238621
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810548G>T , CM000673.2:g.128810548G>T GRCh38
NC_000011.9:g.128680443G>T , CM000673.1:g.128680443G>T GRCh37
NC_000011.8:g.128185653G>T NCBI36
NG_032912.1:g.129014G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.940G>T ENSP00000513017.1:p.Gly314Trp
ENST00000527786.7:c.919G>T MANE Select ENSP00000433488.2:p.Gly307Trp
ENST00000281428.12:c.721G>T ENSP00000281428.8:p.Gly241Trp
ENST00000344954.10:c.340G>T ENSP00000339627.7:p.Gly114Trp
ENST00000429175.7:c.*841G>T ENSP00000399985.3:n.*841G>T
ENST00000527786.6:c.919G>T ENSP00000433488.2:p.Gly307Trp
ENST00000528790.1:n.3502G>T
ENST00000534087.3:c.820G>T ENSP00000432950.1:p.Gly274Trp
ENST00000608303.5:c.*311G>T ENSP00000477262.1:n.*311G>T
NM_001167681.2:c.820G>T NP_001161153.1:p.Gly274Trp
NM_001271010.1:c.721G>T NP_001257939.1:p.Gly241Trp
NM_001271012.1:c.340G>T NP_001257941.1:p.Gly114Trp
NM_002017.4:c.919G>T NP_002008.2:p.Gly307Trp
XM_011542701.1:c.820G>T XP_011541003.1:p.Gly274Trp
XM_011542702.1:c.793G>T XP_011541004.1:p.Gly265Trp
XM_011542701.2:c.820G>T XP_011541003.1:p.Gly274Trp
XM_017017405.1:c.820G>T XP_016872894.1:p.Gly274Trp
XM_017017406.1:c.820G>T XP_016872895.1:p.Gly274Trp
NM_002017.5:c.919G>T MANE Select NP_002008.2:p.Gly307Trp
NM_001167681.3:c.820G>T NP_001161153.1:p.Gly274Trp
NM_001271010.2:c.721G>T NP_001257939.1:p.Gly241Trp
NM_001271012.2:c.340G>T NP_001257941.1:p.Gly114Trp