Canonical Allele Identifier: CA15677042

Gene: FLI1

Linked Data

• dbSNP Id: rs654723
• gnomAD v2: 11-128586155-C-A
• gnomAD v3: 11-128716260-C-A
• gnomAD v4: 11-128716260-C-A
• MyVariant Identifiers: chr11:g.128586155C>A (hg19) ; chr11:g.128716260C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128716260C>A , CM000673.2:g.128716260C>A	GRCh38
NC_000011.9:g.128586155C>A , CM000673.1:g.128586155C>A	GRCh37
NC_000011.8:g.128091365C>A	NCBI36
NG_032912.1:g.34726C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.39+29559C>A	ENSP00000513017.1:n.39+29559C>A
ENST00000527786.7:c.18+21984C>A MANE Select	ENSP00000433488.2:n.18+21984C>A
ENST00000281428.12:c.-352+21984C>A	ENSP00000281428.8:n.-352+21984C>A
ENST00000344954.10:c.-203+29559C>A	ENSP00000339627.7:n.-203+29559C>A
ENST00000429175.7:c.18+21984C>A	ENSP00000399985.3:n.18+21984C>A
ENST00000527767.7:c.-82+23117C>A	ENSP00000476428.1:n.-82+23117C>A
ENST00000527786.6:c.18+21984C>A	ENSP00000433488.2:n.18+21984C>A
ENST00000534087.3:c.-136+21984C>A	ENSP00000432950.1:n.-136+21984C>A
ENST00000608303.5:c.-82+29559C>A	ENSP00000477262.1:n.-82+29559C>A
NM_001167681.2:c.-136+21984C>A	NP_001161153.1:n.-136+21984C>A
NM_001271010.1:c.-352+21984C>A	NP_001257939.1:n.-352+21984C>A
NM_001271012.1:c.-203+29559C>A	NP_001257941.1:n.-203+29559C>A
NM_002017.4:c.18+21984C>A	NP_002008.2:n.18+21984C>A
XM_011542701.1:c.-82+23117C>A	XP_011541003.1:n.-82+23117C>A
XM_011542702.1:c.18+21984C>A	XP_011541004.1:n.18+21984C>A
XR_948171.1:n.1063-197C>A
XM_011542701.2:c.-82+23117C>A	XP_011541003.1:n.-82+23117C>A
XM_017017405.1:c.-82+30888C>A	XP_016872894.1:n.-82+30888C>A
XM_017017406.1:c.-82+23460C>A	XP_016872895.1:n.-82+23460C>A
NM_002017.5:c.18+21984C>A MANE Select	NP_002008.2:n.18+21984C>A
NM_001167681.3:c.-136+21984C>A	NP_001161153.1:n.-136+21984C>A
NM_001271010.2:c.-352+21984C>A	NP_001257939.1:n.-352+21984C>A
NM_001271012.2:c.-203+29559C>A	NP_001257941.1:n.-203+29559C>A