Canonical Allele Identifier: CA477702328

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680385C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810490C>G , CM000673.2:g.128810490C>G	GRCh38
NC_000011.9:g.128680385C>G , CM000673.1:g.128680385C>G	GRCh37
NC_000011.8:g.128185595C>G	NCBI36
NG_032912.1:g.128956C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.882C>G	ENSP00000513017.1:p.Leu294=
ENST00000527786.7:c.861C>G MANE Select	ENSP00000433488.2:p.Leu287=
ENST00000281428.12:c.663C>G	ENSP00000281428.8:p.Leu221=
ENST00000344954.10:c.282C>G	ENSP00000339627.7:p.Leu94=
ENST00000429175.7:c.*783C>G	ENSP00000399985.3:n.*783C>G
ENST00000527786.6:c.861C>G	ENSP00000433488.2:p.Leu287=
ENST00000528790.1:n.3444C>G
ENST00000534087.3:c.762C>G	ENSP00000432950.1:p.Leu254=
ENST00000608303.5:c.*253C>G	ENSP00000477262.1:n.*253C>G
NM_001167681.2:c.762C>G	NP_001161153.1:p.Leu254=
NM_001271010.1:c.663C>G	NP_001257939.1:p.Leu221=
NM_001271012.1:c.282C>G	NP_001257941.1:p.Leu94=
NM_002017.4:c.861C>G	NP_002008.2:p.Leu287=
XM_011542701.1:c.762C>G	XP_011541003.1:p.Leu254=
XM_011542702.1:c.735C>G	XP_011541004.1:p.Leu245=
XM_011542701.2:c.762C>G	XP_011541003.1:p.Leu254=
XM_017017405.1:c.762C>G	XP_016872894.1:p.Leu254=
XM_017017406.1:c.762C>G	XP_016872895.1:p.Leu254=
NM_002017.5:c.861C>G MANE Select	NP_002008.2:p.Leu287=
NM_001167681.3:c.762C>G	NP_001161153.1:p.Leu254=
NM_001271010.2:c.663C>G	NP_001257939.1:p.Leu221=
NM_001271012.2:c.282C>G	NP_001257941.1:p.Leu94=