Canonical Allele Identifier: CA383238452
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810475G>C , CM000673.2:g.128810475G>C GRCh38
NC_000011.9:g.128680370G>C , CM000673.1:g.128680370G>C GRCh37
NC_000011.8:g.128185580G>C NCBI36
NG_032912.1:g.128941G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.867G>C ENSP00000513017.1:p.Gln289His
ENST00000527786.7:c.846G>C MANE Select ENSP00000433488.2:p.Gln282His
ENST00000281428.12:c.648G>C ENSP00000281428.8:p.Gln216His
ENST00000344954.10:c.267G>C ENSP00000339627.7:p.Gln89His
ENST00000429175.7:c.*768G>C ENSP00000399985.3:n.*768G>C
ENST00000527786.6:c.846G>C ENSP00000433488.2:p.Gln282His
ENST00000528790.1:n.3429G>C
ENST00000534087.3:c.747G>C ENSP00000432950.1:p.Gln249His
ENST00000608303.5:c.*238G>C ENSP00000477262.1:n.*238G>C
NM_001167681.2:c.747G>C NP_001161153.1:p.Gln249His
NM_001271010.1:c.648G>C NP_001257939.1:p.Gln216His
NM_001271012.1:c.267G>C NP_001257941.1:p.Gln89His
NM_002017.4:c.846G>C NP_002008.2:p.Gln282His
XM_011542701.1:c.747G>C XP_011541003.1:p.Gln249His
XM_011542702.1:c.720G>C XP_011541004.1:p.Gln240His
XM_011542701.2:c.747G>C XP_011541003.1:p.Gln249His
XM_017017405.1:c.747G>C XP_016872894.1:p.Gln249His
XM_017017406.1:c.747G>C XP_016872895.1:p.Gln249His
NM_002017.5:c.846G>C MANE Select NP_002008.2:p.Gln282His
NM_001167681.3:c.747G>C NP_001161153.1:p.Gln249His
NM_001271010.2:c.648G>C NP_001257939.1:p.Gln216His
NM_001271012.2:c.267G>C NP_001257941.1:p.Gln89His