Canonical Allele Identifier: CA6357288

Gene: FLI1

Linked Data

• dbSNP Id: rs748983663
• ExAC: 11:128680442 C / T
• gnomAD v2: 11-128680442-C-T
• gnomAD v3: 11-128810547-C-T
• gnomAD v4: 11-128810547-C-T
• COSMIC: COSM4019254
• MyVariant Identifiers: chr11:g.128680442C>T (hg19) ; chr11:g.128810547C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810547C>T , CM000673.2:g.128810547C>T	GRCh38
NC_000011.9:g.128680442C>T , CM000673.1:g.128680442C>T	GRCh37
NC_000011.8:g.128185652C>T	NCBI36
NG_032912.1:g.129013C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.939C>T	ENSP00000513017.1:p.Asn313=
ENST00000527786.7:c.918C>T MANE Select	ENSP00000433488.2:p.Asn306=
ENST00000281428.12:c.720C>T	ENSP00000281428.8:p.Asn240=
ENST00000344954.10:c.339C>T	ENSP00000339627.7:p.Asn113=
ENST00000429175.7:c.*840C>T	ENSP00000399985.3:n.*840C>T
ENST00000527786.6:c.918C>T	ENSP00000433488.2:p.Asn306=
ENST00000528790.1:n.3501C>T
ENST00000534087.3:c.819C>T	ENSP00000432950.1:p.Asn273=
ENST00000608303.5:c.*310C>T	ENSP00000477262.1:n.*310C>T
NM_001167681.2:c.819C>T	NP_001161153.1:p.Asn273=
NM_001271010.1:c.720C>T	NP_001257939.1:p.Asn240=
NM_001271012.1:c.339C>T	NP_001257941.1:p.Asn113=
NM_002017.4:c.918C>T	NP_002008.2:p.Asn306=
XM_011542701.1:c.819C>T	XP_011541003.1:p.Asn273=
XM_011542702.1:c.792C>T	XP_011541004.1:p.Asn264=
XM_011542701.2:c.819C>T	XP_011541003.1:p.Asn273=
XM_017017405.1:c.819C>T	XP_016872894.1:p.Asn273=
XM_017017406.1:c.819C>T	XP_016872895.1:p.Asn273=
NM_002017.5:c.918C>T MANE Select	NP_002008.2:p.Asn306=
NM_001167681.3:c.819C>T	NP_001161153.1:p.Asn273=
NM_001271010.2:c.720C>T	NP_001257939.1:p.Asn240=
NM_001271012.2:c.339C>T	NP_001257941.1:p.Asn113=