Canonical Allele Identifier: CA16621535

Gene: FLI1

Linked Data

• ClinVar Variation Id: 424634
• ClinVar RCV Id: RCV000487462 ; RCV001003905 ; RCV001270513
• dbSNP Id: rs1064797085
• MyVariant Identifiers: chr11:g.128680516_128680519del (hg19) ; chr11:g.128810621_128810624del (hg38)
• PubMed: PMID:24100448

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810621_128810624del , CM000673.2:g.128810621_128810624del	GRCh38
NC_000011.9:g.128680516_128680519del , CM000673.1:g.128680516_128680519del	GRCh37
NC_000011.8:g.128185726_128185729del	NCBI36
NG_032912.1:g.129087_129090del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1013_1016del	ENSP00000513017.1:p.Asn338ThrfsTer4
ENST00000527786.7:c.992_995del MANE Select	ENSP00000433488.2:p.Asn331ThrfsTer4
ENST00000281428.12:c.794_797del	ENSP00000281428.8:p.Asn265ThrfsTer4
ENST00000344954.10:c.413_416del	ENSP00000339627.7:p.Asn138ThrfsTer4
ENST00000429175.7:c.*914_*917del	ENSP00000399985.3:n.*914_*917del
ENST00000527786.6:c.992_995del	ENSP00000433488.2:p.Asn331ThrfsTer4
ENST00000528790.1:n.3575_3578del
ENST00000534087.3:c.893_896del	ENSP00000432950.1:p.Asn298ThrfsTer4
ENST00000608303.5:c.*384_*387del	ENSP00000477262.1:n.*384_*387del
NM_001167681.2:c.893_896del	NP_001161153.1:p.Asn298ThrfsTer4
NM_001271010.1:c.794_797del	NP_001257939.1:p.Asn265ThrfsTer4
NM_001271012.1:c.413_416del	NP_001257941.1:p.Asn138ThrfsTer4
NM_002017.4:c.992_995del	NP_002008.2:p.Asn331ThrfsTer4
XM_011542701.1:c.893_896del	XP_011541003.1:p.Asn298ThrfsTer4
XM_011542702.1:c.866_869del	XP_011541004.1:p.Asn289ThrfsTer4
XM_011542701.2:c.893_896del	XP_011541003.1:p.Asn298ThrfsTer4
XM_017017405.1:c.893_896del	XP_016872894.1:p.Asn298ThrfsTer4
XM_017017406.1:c.893_896del	XP_016872895.1:p.Asn298ThrfsTer4
NM_002017.5:c.992_995del MANE Select	NP_002008.2:p.Asn331ThrfsTer4
NM_001167681.3:c.893_896del	NP_001161153.1:p.Asn298ThrfsTer4
NM_001271010.2:c.794_797del	NP_001257939.1:p.Asn265ThrfsTer4
NM_001271012.2:c.413_416del	NP_001257941.1:p.Asn138ThrfsTer4