Canonical Allele Identifier: CA2008248563

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810761A= , CM000673.2:g.128810761A=	GRCh38
NC_000011.9:g.128680656A= , CM000673.1:g.128680656A=	GRCh37
NC_000011.8:g.128185866A=	NCBI36
NG_032912.1:g.129227A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1153A=	ENSP00000513017.1:p.Met385=
ENST00000527786.7:c.1132A= MANE Select	ENSP00000433488.2:p.Met378=
ENST00000281428.12:c.934A=	ENSP00000281428.8:p.Met312=
ENST00000344954.10:c.553A=	ENSP00000339627.7:p.Met185=
ENST00000429175.7:c.*1054A=	ENSP00000399985.3:n.*1054A=
ENST00000527786.6:c.1132A=	ENSP00000433488.2:p.Met378=
ENST00000528790.1:n.3715A=
ENST00000534087.3:c.1033A=	ENSP00000432950.1:p.Met345=
ENST00000608303.5:c.*524A=	ENSP00000477262.1:n.*524A=
NM_001167681.2:c.1033A=	NP_001161153.1:p.Met345=
NM_001271010.1:c.934A=	NP_001257939.1:p.Met312=
NM_001271012.1:c.553A=	NP_001257941.1:p.Met185=
NM_002017.4:c.1132A=	NP_002008.2:p.Met378=
XM_011542701.1:c.1033A=	XP_011541003.1:p.Met345=
XM_011542702.1:c.1006A=	XP_011541004.1:p.Met336=
XM_011542701.2:c.1033A=	XP_011541003.1:p.Met345=
XM_017017405.1:c.1033A=	XP_016872894.1:p.Met345=
XM_017017406.1:c.1033A=	XP_016872895.1:p.Met345=
NM_002017.5:c.1132A= MANE Select	NP_002008.2:p.Met378=
NM_001167681.3:c.1033A=	NP_001161153.1:p.Met345=
NM_001271010.2:c.934A=	NP_001257939.1:p.Met312=
NM_001271012.2:c.553A=	NP_001257941.1:p.Met185=