Canonical Allele Identifier: CA2008248362

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810619_128810623delinsGAATT , CM000673.2:g.128810619_128810623delinsGAATT	GRCh38
NC_000011.9:g.128680514_128680518delinsGAATT , CM000673.1:g.128680514_128680518delinsGAATT	GRCh37
NC_000011.8:g.128185724_128185728delinsGAATT	NCBI36
NG_032912.1:g.129085_129089delinsGAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1011_1015delinsGAATT	ENSP00000513017.1:p.Met337=
ENST00000527786.7:c.990_994delinsGAATT MANE Select	ENSP00000433488.2:p.Met330=
ENST00000281428.12:c.792_796delinsGAATT	ENSP00000281428.8:p.Met264=
ENST00000344954.10:c.411_415delinsGAATT	ENSP00000339627.7:p.Met137=
ENST00000429175.7:c.*912_*916delinsGAATT	ENSP00000399985.3:n.*912_*916delinsGAATT
ENST00000527786.6:c.990_994delinsGAATT	ENSP00000433488.2:p.Met330=
ENST00000528790.1:n.3573_3577delinsGAATT
ENST00000534087.3:c.891_895delinsGAATT	ENSP00000432950.1:p.Met297=
ENST00000608303.5:c.*382_*386delinsGAATT	ENSP00000477262.1:n.*382_*386delinsGAATT
NM_001167681.2:c.891_895delinsGAATT	NP_001161153.1:p.Met297=
NM_001271010.1:c.792_796delinsGAATT	NP_001257939.1:p.Met264=
NM_001271012.1:c.411_415delinsGAATT	NP_001257941.1:p.Met137=
NM_002017.4:c.990_994delinsGAATT	NP_002008.2:p.Met330=
XM_011542701.1:c.891_895delinsGAATT	XP_011541003.1:p.Met297=
XM_011542702.1:c.864_868delinsGAATT	XP_011541004.1:p.Met288=
XM_011542701.2:c.891_895delinsGAATT	XP_011541003.1:p.Met297=
XM_017017405.1:c.891_895delinsGAATT	XP_016872894.1:p.Met297=
XM_017017406.1:c.891_895delinsGAATT	XP_016872895.1:p.Met297=
NM_002017.5:c.990_994delinsGAATT MANE Select	NP_002008.2:p.Met330=
NM_001167681.3:c.891_895delinsGAATT	NP_001161153.1:p.Met297=
NM_001271010.2:c.792_796delinsGAATT	NP_001257939.1:p.Met264=
NM_001271012.2:c.411_415delinsGAATT	NP_001257941.1:p.Met137=