Canonical Allele Identifier: CA383238742
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810600G>T , CM000673.2:g.128810600G>T GRCh38
NC_000011.9:g.128680495G>T , CM000673.1:g.128680495G>T GRCh37
NC_000011.8:g.128185705G>T NCBI36
NG_032912.1:g.129066G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.992G>T ENSP00000513017.1:p.Arg331Leu
ENST00000527786.7:c.971G>T MANE Select ENSP00000433488.2:p.Arg324Leu
ENST00000281428.12:c.773G>T ENSP00000281428.8:p.Arg258Leu
ENST00000344954.10:c.392G>T ENSP00000339627.7:p.Arg131Leu
ENST00000429175.7:c.*893G>T ENSP00000399985.3:n.*893G>T
ENST00000527786.6:c.971G>T ENSP00000433488.2:p.Arg324Leu
ENST00000528790.1:n.3554G>T
ENST00000534087.3:c.872G>T ENSP00000432950.1:p.Arg291Leu
ENST00000608303.5:c.*363G>T ENSP00000477262.1:n.*363G>T
NM_001167681.2:c.872G>T NP_001161153.1:p.Arg291Leu
NM_001271010.1:c.773G>T NP_001257939.1:p.Arg258Leu
NM_001271012.1:c.392G>T NP_001257941.1:p.Arg131Leu
NM_002017.4:c.971G>T NP_002008.2:p.Arg324Leu
XM_011542701.1:c.872G>T XP_011541003.1:p.Arg291Leu
XM_011542702.1:c.845G>T XP_011541004.1:p.Arg282Leu
XM_011542701.2:c.872G>T XP_011541003.1:p.Arg291Leu
XM_017017405.1:c.872G>T XP_016872894.1:p.Arg291Leu
XM_017017406.1:c.872G>T XP_016872895.1:p.Arg291Leu
NM_002017.5:c.971G>T MANE Select NP_002008.2:p.Arg324Leu
NM_001167681.3:c.872G>T NP_001161153.1:p.Arg291Leu
NM_001271010.2:c.773G>T NP_001257939.1:p.Arg258Leu
NM_001271012.2:c.392G>T NP_001257941.1:p.Arg131Leu