Canonical Allele Identifier: CA383238611

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680440A>C (hg19) ; chr11:g.128810545A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810545A>C , CM000673.2:g.128810545A>C	GRCh38
NC_000011.9:g.128680440A>C , CM000673.1:g.128680440A>C	GRCh37
NC_000011.8:g.128185650A>C	NCBI36
NG_032912.1:g.129011A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.937A>C	ENSP00000513017.1:p.Asn313His
ENST00000527786.7:c.916A>C MANE Select	ENSP00000433488.2:p.Asn306His
ENST00000281428.12:c.718A>C	ENSP00000281428.8:p.Asn240His
ENST00000344954.10:c.337A>C	ENSP00000339627.7:p.Asn113His
ENST00000429175.7:c.*838A>C	ENSP00000399985.3:n.*838A>C
ENST00000527786.6:c.916A>C	ENSP00000433488.2:p.Asn306His
ENST00000528790.1:n.3499A>C
ENST00000534087.3:c.817A>C	ENSP00000432950.1:p.Asn273His
ENST00000608303.5:c.*308A>C	ENSP00000477262.1:n.*308A>C
NM_001167681.2:c.817A>C	NP_001161153.1:p.Asn273His
NM_001271010.1:c.718A>C	NP_001257939.1:p.Asn240His
NM_001271012.1:c.337A>C	NP_001257941.1:p.Asn113His
NM_002017.4:c.916A>C	NP_002008.2:p.Asn306His
XM_011542701.1:c.817A>C	XP_011541003.1:p.Asn273His
XM_011542702.1:c.790A>C	XP_011541004.1:p.Asn264His
XM_011542701.2:c.817A>C	XP_011541003.1:p.Asn273His
XM_017017405.1:c.817A>C	XP_016872894.1:p.Asn273His
XM_017017406.1:c.817A>C	XP_016872895.1:p.Asn273His
NM_002017.5:c.916A>C MANE Select	NP_002008.2:p.Asn306His
NM_001167681.3:c.817A>C	NP_001161153.1:p.Asn273His
NM_001271010.2:c.718A>C	NP_001257939.1:p.Asn240His
NM_001271012.2:c.337A>C	NP_001257941.1:p.Asn113His