Canonical Allele Identifier: CA477702261

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680367C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810472C>A , CM000673.2:g.128810472C>A	GRCh38
NC_000011.9:g.128680367C>A , CM000673.1:g.128680367C>A	GRCh37
NC_000011.8:g.128185577C>A	NCBI36
NG_032912.1:g.128938C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.864C>A	ENSP00000513017.1:p.Ile288=
ENST00000527786.7:c.843C>A MANE Select	ENSP00000433488.2:p.Ile281=
ENST00000281428.12:c.645C>A	ENSP00000281428.8:p.Ile215=
ENST00000344954.10:c.264C>A	ENSP00000339627.7:p.Ile88=
ENST00000429175.7:c.*765C>A	ENSP00000399985.3:n.*765C>A
ENST00000527786.6:c.843C>A	ENSP00000433488.2:p.Ile281=
ENST00000528790.1:n.3426C>A
ENST00000534087.3:c.744C>A	ENSP00000432950.1:p.Ile248=
ENST00000608303.5:c.*235C>A	ENSP00000477262.1:n.*235C>A
NM_001167681.2:c.744C>A	NP_001161153.1:p.Ile248=
NM_001271010.1:c.645C>A	NP_001257939.1:p.Ile215=
NM_001271012.1:c.264C>A	NP_001257941.1:p.Ile88=
NM_002017.4:c.843C>A	NP_002008.2:p.Ile281=
XM_011542701.1:c.744C>A	XP_011541003.1:p.Ile248=
XM_011542702.1:c.717C>A	XP_011541004.1:p.Ile239=
XM_011542701.2:c.744C>A	XP_011541003.1:p.Ile248=
XM_017017405.1:c.744C>A	XP_016872894.1:p.Ile248=
XM_017017406.1:c.744C>A	XP_016872895.1:p.Ile248=
NM_002017.5:c.843C>A MANE Select	NP_002008.2:p.Ile281=
NM_001167681.3:c.744C>A	NP_001161153.1:p.Ile248=
NM_001271010.2:c.645C>A	NP_001257939.1:p.Ile215=
NM_001271012.2:c.264C>A	NP_001257941.1:p.Ile88=