Canonical Allele Identifier: CA13433235

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128745591A>G , CM000673.2:g.128745591A>G	GRCh38
NC_000011.9:g.128615486A>G , CM000673.1:g.128615486A>G	GRCh37
NC_000011.8:g.128120696A>G	NCBI36
NG_032912.1:g.64057A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002017.5:c.19-12524A>G MANE Select	NP_002008.2:n.19-12524A>G
ENST00000527786.7:c.19-12524A>G MANE Select	ENSP00000433488.2:n.19-12524A>G
NM_001167681.2:c.-135-2646A>G	NP_001161153.1:n.-135-2646A>G
NM_001167681.3:c.-135-2646A>G	NP_001161153.1:n.-135-2646A>G
NM_001271010.1:c.-351-12524A>G	NP_001257939.1:n.-351-12524A>G
NM_001271010.2:c.-351-12524A>G	NP_001257939.1:n.-351-12524A>G
NM_001271012.1:c.-202-12524A>G	NP_001257941.1:n.-202-12524A>G
NM_001271012.2:c.-202-12524A>G	NP_001257941.1:n.-202-12524A>G
NM_002017.4:c.19-12524A>G	NP_002008.2:n.19-12524A>G
ENST00000281428.12:c.-351-12524A>G	ENSP00000281428.8:n.-351-12524A>G
ENST00000344954.10:c.-202-12524A>G	ENSP00000339627.7:n.-202-12524A>G
ENST00000429175.7:c.19-12524A>G	ENSP00000399985.3:n.19-12524A>G
ENST00000527767.7:c.-81-12524A>G	ENSP00000476428.1:n.-81-12524A>G
ENST00000527786.6:c.19-12524A>G	ENSP00000433488.2:n.19-12524A>G
ENST00000534087.3:c.-135-2646A>G	ENSP00000432950.1:n.-135-2646A>G
ENST00000608303.5:c.-81-12524A>G	ENSP00000477262.1:n.-81-12524A>G
ENST00000696982.1:c.40-12524A>G	ENSP00000513017.1:n.40-12524A>G
XM_011542701.1:c.-81-12524A>G	XP_011541003.1:n.-81-12524A>G
XM_011542701.2:c.-81-12524A>G	XP_011541003.1:n.-81-12524A>G
XM_011542702.1:c.19-12524A>G	XP_011541004.1:n.19-12524A>G
XM_017017405.1:c.-81-12524A>G	XP_016872894.1:n.-81-12524A>G
XM_017017406.1:c.-81-12524A>G	XP_016872895.1:n.-81-12524A>G