Canonical Allele Identifier: CA477702335

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680388G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810493G>C , CM000673.2:g.128810493G>C	GRCh38
NC_000011.9:g.128680388G>C , CM000673.1:g.128680388G>C	GRCh37
NC_000011.8:g.128185598G>C	NCBI36
NG_032912.1:g.128959G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.885G>C	ENSP00000513017.1:p.Leu295=
ENST00000527786.7:c.864G>C MANE Select	ENSP00000433488.2:p.Leu288=
ENST00000281428.12:c.666G>C	ENSP00000281428.8:p.Leu222=
ENST00000344954.10:c.285G>C	ENSP00000339627.7:p.Leu95=
ENST00000429175.7:c.*786G>C	ENSP00000399985.3:n.*786G>C
ENST00000527786.6:c.864G>C	ENSP00000433488.2:p.Leu288=
ENST00000528790.1:n.3447G>C
ENST00000534087.3:c.765G>C	ENSP00000432950.1:p.Leu255=
ENST00000608303.5:c.*256G>C	ENSP00000477262.1:n.*256G>C
NM_001167681.2:c.765G>C	NP_001161153.1:p.Leu255=
NM_001271010.1:c.666G>C	NP_001257939.1:p.Leu222=
NM_001271012.1:c.285G>C	NP_001257941.1:p.Leu95=
NM_002017.4:c.864G>C	NP_002008.2:p.Leu288=
XM_011542701.1:c.765G>C	XP_011541003.1:p.Leu255=
XM_011542702.1:c.738G>C	XP_011541004.1:p.Leu246=
XM_011542701.2:c.765G>C	XP_011541003.1:p.Leu255=
XM_017017405.1:c.765G>C	XP_016872894.1:p.Leu255=
XM_017017406.1:c.765G>C	XP_016872895.1:p.Leu255=
NM_002017.5:c.864G>C MANE Select	NP_002008.2:p.Leu288=
NM_001167681.3:c.765G>C	NP_001161153.1:p.Leu255=
NM_001271010.2:c.666G>C	NP_001257939.1:p.Leu222=
NM_001271012.2:c.285G>C	NP_001257941.1:p.Leu95=