Canonical Allele Identifier: CA383238699

Gene: FLI1

Linked Data

• gnomAD v4: 11-128810581-G-A
• MyVariant Identifiers: chr11:g.128680476G>A (hg19) ; chr11:g.128810581G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810581G>A , CM000673.2:g.128810581G>A	GRCh38
NC_000011.9:g.128680476G>A , CM000673.1:g.128680476G>A	GRCh37
NC_000011.8:g.128185686G>A	NCBI36
NG_032912.1:g.129047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.973G>A	ENSP00000513017.1:p.Ala325Thr
ENST00000527786.7:c.952G>A MANE Select	ENSP00000433488.2:p.Ala318Thr
ENST00000281428.12:c.754G>A	ENSP00000281428.8:p.Ala252Thr
ENST00000344954.10:c.373G>A	ENSP00000339627.7:p.Ala125Thr
ENST00000429175.7:c.*874G>A	ENSP00000399985.3:n.*874G>A
ENST00000527786.6:c.952G>A	ENSP00000433488.2:p.Ala318Thr
ENST00000528790.1:n.3535G>A
ENST00000534087.3:c.853G>A	ENSP00000432950.1:p.Ala285Thr
ENST00000608303.5:c.*344G>A	ENSP00000477262.1:n.*344G>A
NM_001167681.2:c.853G>A	NP_001161153.1:p.Ala285Thr
NM_001271010.1:c.754G>A	NP_001257939.1:p.Ala252Thr
NM_001271012.1:c.373G>A	NP_001257941.1:p.Ala125Thr
NM_002017.4:c.952G>A	NP_002008.2:p.Ala318Thr
XM_011542701.1:c.853G>A	XP_011541003.1:p.Ala285Thr
XM_011542702.1:c.826G>A	XP_011541004.1:p.Ala276Thr
XM_011542701.2:c.853G>A	XP_011541003.1:p.Ala285Thr
XM_017017405.1:c.853G>A	XP_016872894.1:p.Ala285Thr
XM_017017406.1:c.853G>A	XP_016872895.1:p.Ala285Thr
NM_002017.5:c.952G>A MANE Select	NP_002008.2:p.Ala318Thr
NM_001167681.3:c.853G>A	NP_001161153.1:p.Ala285Thr
NM_001271010.2:c.754G>A	NP_001257939.1:p.Ala252Thr
NM_001271012.2:c.373G>A	NP_001257941.1:p.Ala125Thr