Canonical Allele Identifier: CA383238730

Gene: FLI1

Linked Data

• COSMIC: COSM3808773 ; COSM5831701
• MyVariant Identifiers: chr11:g.128680489G>A (hg19) ; chr11:g.128810594G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810594G>A , CM000673.2:g.128810594G>A	GRCh38
NC_000011.9:g.128680489G>A , CM000673.1:g.128680489G>A	GRCh37
NC_000011.8:g.128185699G>A	NCBI36
NG_032912.1:g.129060G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.986G>A	ENSP00000513017.1:p.Gly329Asp
ENST00000527786.7:c.965G>A MANE Select	ENSP00000433488.2:p.Gly322Asp
ENST00000281428.12:c.767G>A	ENSP00000281428.8:p.Gly256Asp
ENST00000344954.10:c.386G>A	ENSP00000339627.7:p.Gly129Asp
ENST00000429175.7:c.*887G>A	ENSP00000399985.3:n.*887G>A
ENST00000527786.6:c.965G>A	ENSP00000433488.2:p.Gly322Asp
ENST00000528790.1:n.3548G>A
ENST00000534087.3:c.866G>A	ENSP00000432950.1:p.Gly289Asp
ENST00000608303.5:c.*357G>A	ENSP00000477262.1:n.*357G>A
NM_001167681.2:c.866G>A	NP_001161153.1:p.Gly289Asp
NM_001271010.1:c.767G>A	NP_001257939.1:p.Gly256Asp
NM_001271012.1:c.386G>A	NP_001257941.1:p.Gly129Asp
NM_002017.4:c.965G>A	NP_002008.2:p.Gly322Asp
XM_011542701.1:c.866G>A	XP_011541003.1:p.Gly289Asp
XM_011542702.1:c.839G>A	XP_011541004.1:p.Gly280Asp
XM_011542701.2:c.866G>A	XP_011541003.1:p.Gly289Asp
XM_017017405.1:c.866G>A	XP_016872894.1:p.Gly289Asp
XM_017017406.1:c.866G>A	XP_016872895.1:p.Gly289Asp
NM_002017.5:c.965G>A MANE Select	NP_002008.2:p.Gly322Asp
NM_001167681.3:c.866G>A	NP_001161153.1:p.Gly289Asp
NM_001271010.2:c.767G>A	NP_001257939.1:p.Gly256Asp
NM_001271012.2:c.386G>A	NP_001257941.1:p.Gly129Asp