Canonical Allele Identifier: CA383238442

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680366T>A (hg19) ; chr11:g.128810471T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810471T>A , CM000673.2:g.128810471T>A	GRCh38
NC_000011.9:g.128680366T>A , CM000673.1:g.128680366T>A	GRCh37
NC_000011.8:g.128185576T>A	NCBI36
NG_032912.1:g.128937T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.863T>A	ENSP00000513017.1:p.Ile288Asn
ENST00000527786.7:c.842T>A MANE Select	ENSP00000433488.2:p.Ile281Asn
ENST00000281428.12:c.644T>A	ENSP00000281428.8:p.Ile215Asn
ENST00000344954.10:c.263T>A	ENSP00000339627.7:p.Ile88Asn
ENST00000429175.7:c.*764T>A	ENSP00000399985.3:n.*764T>A
ENST00000527786.6:c.842T>A	ENSP00000433488.2:p.Ile281Asn
ENST00000528790.1:n.3425T>A
ENST00000534087.3:c.743T>A	ENSP00000432950.1:p.Ile248Asn
ENST00000608303.5:c.*234T>A	ENSP00000477262.1:n.*234T>A
NM_001167681.2:c.743T>A	NP_001161153.1:p.Ile248Asn
NM_001271010.1:c.644T>A	NP_001257939.1:p.Ile215Asn
NM_001271012.1:c.263T>A	NP_001257941.1:p.Ile88Asn
NM_002017.4:c.842T>A	NP_002008.2:p.Ile281Asn
XM_011542701.1:c.743T>A	XP_011541003.1:p.Ile248Asn
XM_011542702.1:c.716T>A	XP_011541004.1:p.Ile239Asn
XM_011542701.2:c.743T>A	XP_011541003.1:p.Ile248Asn
XM_017017405.1:c.743T>A	XP_016872894.1:p.Ile248Asn
XM_017017406.1:c.743T>A	XP_016872895.1:p.Ile248Asn
NM_002017.5:c.842T>A MANE Select	NP_002008.2:p.Ile281Asn
NM_001167681.3:c.743T>A	NP_001161153.1:p.Ile248Asn
NM_001271010.2:c.644T>A	NP_001257939.1:p.Ile215Asn
NM_001271012.2:c.263T>A	NP_001257941.1:p.Ile88Asn