Canonical Allele Identifier: CA477702516

Gene: FLI1

Linked Data

• gnomAD v4: 11-128810586-G-A
• MyVariant Identifiers: chr11:g.128680481G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810586G>A , CM000673.2:g.128810586G>A	GRCh38
NC_000011.9:g.128680481G>A , CM000673.1:g.128680481G>A	GRCh37
NC_000011.8:g.128185691G>A	NCBI36
NG_032912.1:g.129052G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.978G>A	ENSP00000513017.1:p.Arg326=
ENST00000527786.7:c.957G>A MANE Select	ENSP00000433488.2:p.Arg319=
ENST00000281428.12:c.759G>A	ENSP00000281428.8:p.Arg253=
ENST00000344954.10:c.378G>A	ENSP00000339627.7:p.Arg126=
ENST00000429175.7:c.*879G>A	ENSP00000399985.3:n.*879G>A
ENST00000527786.6:c.957G>A	ENSP00000433488.2:p.Arg319=
ENST00000528790.1:n.3540G>A
ENST00000534087.3:c.858G>A	ENSP00000432950.1:p.Arg286=
ENST00000608303.5:c.*349G>A	ENSP00000477262.1:n.*349G>A
NM_001167681.2:c.858G>A	NP_001161153.1:p.Arg286=
NM_001271010.1:c.759G>A	NP_001257939.1:p.Arg253=
NM_001271012.1:c.378G>A	NP_001257941.1:p.Arg126=
NM_002017.4:c.957G>A	NP_002008.2:p.Arg319=
XM_011542701.1:c.858G>A	XP_011541003.1:p.Arg286=
XM_011542702.1:c.831G>A	XP_011541004.1:p.Arg277=
XM_011542701.2:c.858G>A	XP_011541003.1:p.Arg286=
XM_017017405.1:c.858G>A	XP_016872894.1:p.Arg286=
XM_017017406.1:c.858G>A	XP_016872895.1:p.Arg286=
NM_002017.5:c.957G>A MANE Select	NP_002008.2:p.Arg319=
NM_001167681.3:c.858G>A	NP_001161153.1:p.Arg286=
NM_001271010.2:c.759G>A	NP_001257939.1:p.Arg253=
NM_001271012.2:c.378G>A	NP_001257941.1:p.Arg126=