Canonical Allele Identifier: CA16621533
Gene: FLI1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424632
ClinVar RCV Id: RCV000487466
dbSNP Id: rs1064797083

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810638C>T , CM000673.2:g.128810638C>T GRCh38
NC_000011.9:g.128680533C>T , CM000673.1:g.128680533C>T GRCh37
NC_000011.8:g.128185743C>T NCBI36
NG_032912.1:g.129104C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696982.1:c.1030C>T ENSP00000513017.1:p.Arg344Trp
ENST00000527786.7:c.1009C>T MANE Select ENSP00000433488.2:p.Arg337Trp
ENST00000281428.12:c.811C>T ENSP00000281428.8:p.Arg271Trp
ENST00000344954.10:c.430C>T ENSP00000339627.7:p.Arg144Trp
ENST00000429175.7:c.*931C>T ENSP00000399985.3:n.*931C>T
ENST00000527786.6:c.1009C>T ENSP00000433488.2:p.Arg337Trp
ENST00000528790.1:n.3592C>T
ENST00000534087.3:c.910C>T ENSP00000432950.1:p.Arg304Trp
ENST00000608303.5:c.*401C>T ENSP00000477262.1:n.*401C>T
NM_001167681.2:c.910C>T NP_001161153.1:p.Arg304Trp
NM_001271010.1:c.811C>T NP_001257939.1:p.Arg271Trp
NM_001271012.1:c.430C>T NP_001257941.1:p.Arg144Trp
NM_002017.4:c.1009C>T NP_002008.2:p.Arg337Trp
XM_011542701.1:c.910C>T XP_011541003.1:p.Arg304Trp
XM_011542702.1:c.883C>T XP_011541004.1:p.Arg295Trp
XM_011542701.2:c.910C>T XP_011541003.1:p.Arg304Trp
XM_017017405.1:c.910C>T XP_016872894.1:p.Arg304Trp
XM_017017406.1:c.910C>T XP_016872895.1:p.Arg304Trp
NM_002017.5:c.1009C>T MANE Select NP_002008.2:p.Arg337Trp
NM_001167681.3:c.910C>T NP_001161153.1:p.Arg304Trp
NM_001271010.2:c.811C>T NP_001257939.1:p.Arg271Trp
NM_001271012.2:c.430C>T NP_001257941.1:p.Arg144Trp