Canonical Allele Identifier: CA6357285

Gene: FLI1

Linked Data

• dbSNP Id: rs748615215
• ExAC: 11:128680408 C / A
• gnomAD v2: 11-128680408-C-A
• gnomAD v4: 11-128810513-C-A
• MyVariant Identifiers: chr11:g.128680408C>A (hg19) ; chr11:g.128810513C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810513C>A , CM000673.2:g.128810513C>A	GRCh38
NC_000011.9:g.128680408C>A , CM000673.1:g.128680408C>A	GRCh37
NC_000011.8:g.128185618C>A	NCBI36
NG_032912.1:g.128979C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.905C>A	ENSP00000513017.1:p.Ala302Asp
ENST00000527786.7:c.884C>A MANE Select	ENSP00000433488.2:p.Ala295Asp
ENST00000281428.12:c.686C>A	ENSP00000281428.8:p.Ala229Asp
ENST00000344954.10:c.305C>A	ENSP00000339627.7:p.Ala102Asp
ENST00000429175.7:c.*806C>A	ENSP00000399985.3:n.*806C>A
ENST00000527786.6:c.884C>A	ENSP00000433488.2:p.Ala295Asp
ENST00000528790.1:n.3467C>A
ENST00000534087.3:c.785C>A	ENSP00000432950.1:p.Ala262Asp
ENST00000608303.5:c.*276C>A	ENSP00000477262.1:n.*276C>A
NM_001167681.2:c.785C>A	NP_001161153.1:p.Ala262Asp
NM_001271010.1:c.686C>A	NP_001257939.1:p.Ala229Asp
NM_001271012.1:c.305C>A	NP_001257941.1:p.Ala102Asp
NM_002017.4:c.884C>A	NP_002008.2:p.Ala295Asp
XM_011542701.1:c.785C>A	XP_011541003.1:p.Ala262Asp
XM_011542702.1:c.758C>A	XP_011541004.1:p.Ala253Asp
XM_011542701.2:c.785C>A	XP_011541003.1:p.Ala262Asp
XM_017017405.1:c.785C>A	XP_016872894.1:p.Ala262Asp
XM_017017406.1:c.785C>A	XP_016872895.1:p.Ala262Asp
NM_002017.5:c.884C>A MANE Select	NP_002008.2:p.Ala295Asp
NM_001167681.3:c.785C>A	NP_001161153.1:p.Ala262Asp
NM_001271010.2:c.686C>A	NP_001257939.1:p.Ala229Asp
NM_001271012.2:c.305C>A	NP_001257941.1:p.Ala102Asp