Canonical Allele Identifier: CA383238840

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680537C>A (hg19) ; chr11:g.128810642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810642C>A , CM000673.2:g.128810642C>A	GRCh38
NC_000011.9:g.128680537C>A , CM000673.1:g.128680537C>A	GRCh37
NC_000011.8:g.128185747C>A	NCBI36
NG_032912.1:g.129108C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1034C>A	ENSP00000513017.1:p.Ala345Asp
ENST00000527786.7:c.1013C>A MANE Select	ENSP00000433488.2:p.Ala338Asp
ENST00000281428.12:c.815C>A	ENSP00000281428.8:p.Ala272Asp
ENST00000344954.10:c.434C>A	ENSP00000339627.7:p.Ala145Asp
ENST00000429175.7:c.*935C>A	ENSP00000399985.3:n.*935C>A
ENST00000527786.6:c.1013C>A	ENSP00000433488.2:p.Ala338Asp
ENST00000528790.1:n.3596C>A
ENST00000534087.3:c.914C>A	ENSP00000432950.1:p.Ala305Asp
ENST00000608303.5:c.*405C>A	ENSP00000477262.1:n.*405C>A
NM_001167681.2:c.914C>A	NP_001161153.1:p.Ala305Asp
NM_001271010.1:c.815C>A	NP_001257939.1:p.Ala272Asp
NM_001271012.1:c.434C>A	NP_001257941.1:p.Ala145Asp
NM_002017.4:c.1013C>A	NP_002008.2:p.Ala338Asp
XM_011542701.1:c.914C>A	XP_011541003.1:p.Ala305Asp
XM_011542702.1:c.887C>A	XP_011541004.1:p.Ala296Asp
XM_011542701.2:c.914C>A	XP_011541003.1:p.Ala305Asp
XM_017017405.1:c.914C>A	XP_016872894.1:p.Ala305Asp
XM_017017406.1:c.914C>A	XP_016872895.1:p.Ala305Asp
NM_002017.5:c.1013C>A MANE Select	NP_002008.2:p.Ala338Asp
NM_001167681.3:c.914C>A	NP_001161153.1:p.Ala305Asp
NM_001271010.2:c.815C>A	NP_001257939.1:p.Ala272Asp
NM_001271012.2:c.434C>A	NP_001257941.1:p.Ala145Asp