Canonical Allele Identifier: CA383238776

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680510A>C (hg19) ; chr11:g.128810615A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810615A>C , CM000673.2:g.128810615A>C	GRCh38
NC_000011.9:g.128680510A>C , CM000673.1:g.128680510A>C	GRCh37
NC_000011.8:g.128185720A>C	NCBI36
NG_032912.1:g.129081A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1007A>C	ENSP00000513017.1:p.Asn336Thr
ENST00000527786.7:c.986A>C MANE Select	ENSP00000433488.2:p.Asn329Thr
ENST00000281428.12:c.788A>C	ENSP00000281428.8:p.Asn263Thr
ENST00000344954.10:c.407A>C	ENSP00000339627.7:p.Asn136Thr
ENST00000429175.7:c.*908A>C	ENSP00000399985.3:n.*908A>C
ENST00000527786.6:c.986A>C	ENSP00000433488.2:p.Asn329Thr
ENST00000528790.1:n.3569A>C
ENST00000534087.3:c.887A>C	ENSP00000432950.1:p.Asn296Thr
ENST00000608303.5:c.*378A>C	ENSP00000477262.1:n.*378A>C
NM_001167681.2:c.887A>C	NP_001161153.1:p.Asn296Thr
NM_001271010.1:c.788A>C	NP_001257939.1:p.Asn263Thr
NM_001271012.1:c.407A>C	NP_001257941.1:p.Asn136Thr
NM_002017.4:c.986A>C	NP_002008.2:p.Asn329Thr
XM_011542701.1:c.887A>C	XP_011541003.1:p.Asn296Thr
XM_011542702.1:c.860A>C	XP_011541004.1:p.Asn287Thr
XM_011542701.2:c.887A>C	XP_011541003.1:p.Asn296Thr
XM_017017405.1:c.887A>C	XP_016872894.1:p.Asn296Thr
XM_017017406.1:c.887A>C	XP_016872895.1:p.Asn296Thr
NM_002017.5:c.986A>C MANE Select	NP_002008.2:p.Asn329Thr
NM_001167681.3:c.887A>C	NP_001161153.1:p.Asn296Thr
NM_001271010.2:c.788A>C	NP_001257939.1:p.Asn263Thr
NM_001271012.2:c.407A>C	NP_001257941.1:p.Asn136Thr