Canonical Allele Identifier: CA2008248477

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810685C= , CM000673.2:g.128810685C=	GRCh38
NC_000011.9:g.128680580C= , CM000673.1:g.128680580C=	GRCh37
NC_000011.8:g.128185790C=	NCBI36
NG_032912.1:g.129151C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1077C=	ENSP00000513017.1:p.His359=
ENST00000527786.7:c.1056C= MANE Select	ENSP00000433488.2:p.His352=
ENST00000281428.12:c.858C=	ENSP00000281428.8:p.His286=
ENST00000344954.10:c.477C=	ENSP00000339627.7:p.His159=
ENST00000429175.7:c.*978C=	ENSP00000399985.3:n.*978C=
ENST00000527786.6:c.1056C=	ENSP00000433488.2:p.His352=
ENST00000528790.1:n.3639C=
ENST00000534087.3:c.957C=	ENSP00000432950.1:p.His319=
ENST00000608303.5:c.*448C=	ENSP00000477262.1:n.*448C=
NM_001167681.2:c.957C=	NP_001161153.1:p.His319=
NM_001271010.1:c.858C=	NP_001257939.1:p.His286=
NM_001271012.1:c.477C=	NP_001257941.1:p.His159=
NM_002017.4:c.1056C=	NP_002008.2:p.His352=
XM_011542701.1:c.957C=	XP_011541003.1:p.His319=
XM_011542702.1:c.930C=	XP_011541004.1:p.His310=
XM_011542701.2:c.957C=	XP_011541003.1:p.His319=
XM_017017405.1:c.957C=	XP_016872894.1:p.His319=
XM_017017406.1:c.957C=	XP_016872895.1:p.His319=
NM_002017.5:c.1056C= MANE Select	NP_002008.2:p.His352=
NM_001167681.3:c.957C=	NP_001161153.1:p.His319=
NM_001271010.2:c.858C=	NP_001257939.1:p.His286=
NM_001271012.2:c.477C=	NP_001257941.1:p.His159=