Canonical Allele Identifier: CA602585818

Gene: FLI1

Linked Data

• dbSNP Id: rs1220534435
• gnomAD v2: 11-128680562-CATT-C
• MyVariant Identifiers: chr11:g.128680563_128680565del (hg19) ; chr11:g.128810668_128810670del (hg38)
• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810670_128810672del , CM000673.2:g.128810670_128810672del	GRCh38
NC_000011.9:g.128680565_128680567del , CM000673.1:g.128680565_128680567del	GRCh37
NC_000011.8:g.128185775_128185777del	NCBI36
NG_032912.1:g.129136_129138del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1062_1064del	ENSP00000513017.1:p.Ile354del
ENST00000527786.7:c.1041_1043del MANE Select	ENSP00000433488.2:p.Ile347del
ENST00000281428.12:c.843_845del	ENSP00000281428.8:p.Ile281del
ENST00000344954.10:c.462_464del	ENSP00000339627.7:p.Ile154del
ENST00000429175.7:c.*963_*965del	ENSP00000399985.3:n.*963_*965del
ENST00000527786.6:c.1041_1043del	ENSP00000433488.2:p.Ile347del
ENST00000528790.1:n.3624_3626del
ENST00000534087.3:c.942_944del	ENSP00000432950.1:p.Ile314del
ENST00000608303.5:c.*433_*435del	ENSP00000477262.1:n.*433_*435del
NM_001167681.2:c.942_944del	NP_001161153.1:p.Ile314del
NM_001271010.1:c.843_845del	NP_001257939.1:p.Ile281del
NM_001271012.1:c.462_464del	NP_001257941.1:p.Ile154del
NM_002017.4:c.1041_1043del	NP_002008.2:p.Ile347del
XM_011542701.1:c.942_944del	XP_011541003.1:p.Ile314del
XM_011542702.1:c.915_917del	XP_011541004.1:p.Ile305del
XM_011542701.2:c.942_944del	XP_011541003.1:p.Ile314del
XM_017017405.1:c.942_944del	XP_016872894.1:p.Ile314del
XM_017017406.1:c.942_944del	XP_016872895.1:p.Ile314del
NM_002017.5:c.1041_1043del MANE Select	NP_002008.2:p.Ile347del
NM_001167681.3:c.942_944del	NP_001161153.1:p.Ile314del
NM_001271010.2:c.843_845del	NP_001257939.1:p.Ile281del
NM_001271012.2:c.462_464del	NP_001257941.1:p.Ile154del