Canonical Allele Identifier: CA2008248163

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810484A= , CM000673.2:g.128810484A=	GRCh38
NC_000011.9:g.128680379A= , CM000673.1:g.128680379A=	GRCh37
NC_000011.8:g.128185589A=	NCBI36
NG_032912.1:g.128950A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.876A=	ENSP00000513017.1:p.Gln292=
ENST00000527786.7:c.855A= MANE Select	ENSP00000433488.2:p.Gln285=
ENST00000281428.12:c.657A=	ENSP00000281428.8:p.Gln219=
ENST00000344954.10:c.276A=	ENSP00000339627.7:p.Gln92=
ENST00000429175.7:c.*777A=	ENSP00000399985.3:n.*777A=
ENST00000527786.6:c.855A=	ENSP00000433488.2:p.Gln285=
ENST00000528790.1:n.3438A=
ENST00000534087.3:c.756A=	ENSP00000432950.1:p.Gln252=
ENST00000608303.5:c.*247A=	ENSP00000477262.1:n.*247A=
NM_001167681.2:c.756A=	NP_001161153.1:p.Gln252=
NM_001271010.1:c.657A=	NP_001257939.1:p.Gln219=
NM_001271012.1:c.276A=	NP_001257941.1:p.Gln92=
NM_002017.4:c.855A=	NP_002008.2:p.Gln285=
XM_011542701.1:c.756A=	XP_011541003.1:p.Gln252=
XM_011542702.1:c.729A=	XP_011541004.1:p.Gln243=
XM_011542701.2:c.756A=	XP_011541003.1:p.Gln252=
XM_017017405.1:c.756A=	XP_016872894.1:p.Gln252=
XM_017017406.1:c.756A=	XP_016872895.1:p.Gln252=
NM_002017.5:c.855A= MANE Select	NP_002008.2:p.Gln285=
NM_001167681.3:c.756A=	NP_001161153.1:p.Gln252=
NM_001271010.2:c.657A=	NP_001257939.1:p.Gln219=
NM_001271012.2:c.276A=	NP_001257941.1:p.Gln92=