Canonical Allele Identifier: CA383239141
Gene: FLI1 HGNC NCBI

Linked Data

dbSNP Id: rs1472717533

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810771A>T , CM000673.2:g.128810771A>T GRCh38
NC_000011.9:g.128680666A>T , CM000673.1:g.128680666A>T GRCh37
NC_000011.8:g.128185876A>T NCBI36
NG_032912.1:g.129237A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1163A>T ENSP00000513017.1:p.Tyr388Phe
ENST00000527786.7:c.1142A>T MANE Select ENSP00000433488.2:p.Tyr381Phe
ENST00000281428.12:c.944A>T ENSP00000281428.8:p.Tyr315Phe
ENST00000344954.10:c.563A>T ENSP00000339627.7:p.Tyr188Phe
ENST00000429175.7:c.*1064A>T ENSP00000399985.3:n.*1064A>T
ENST00000527786.6:c.1142A>T ENSP00000433488.2:p.Tyr381Phe
ENST00000528790.1:n.3725A>T
ENST00000534087.3:c.1043A>T ENSP00000432950.1:p.Tyr348Phe
ENST00000608303.5:c.*534A>T ENSP00000477262.1:n.*534A>T
NM_001167681.2:c.1043A>T NP_001161153.1:p.Tyr348Phe
NM_001271010.1:c.944A>T NP_001257939.1:p.Tyr315Phe
NM_001271012.1:c.563A>T NP_001257941.1:p.Tyr188Phe
NM_002017.4:c.1142A>T NP_002008.2:p.Tyr381Phe
XM_011542701.1:c.1043A>T XP_011541003.1:p.Tyr348Phe
XM_011542702.1:c.1016A>T XP_011541004.1:p.Tyr339Phe
XM_011542701.2:c.1043A>T XP_011541003.1:p.Tyr348Phe
XM_017017405.1:c.1043A>T XP_016872894.1:p.Tyr348Phe
XM_017017406.1:c.1043A>T XP_016872895.1:p.Tyr348Phe
NM_002017.5:c.1142A>T MANE Select NP_002008.2:p.Tyr381Phe
NM_001167681.3:c.1043A>T NP_001161153.1:p.Tyr348Phe
NM_001271010.2:c.944A>T NP_001257939.1:p.Tyr315Phe
NM_001271012.2:c.563A>T NP_001257941.1:p.Tyr188Phe