Canonical Allele Identifier: CA2008248526

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810742A= , CM000673.2:g.128810742A=	GRCh38
NC_000011.9:g.128680637A= , CM000673.1:g.128680637A=	GRCh37
NC_000011.8:g.128185847A=	NCBI36
NG_032912.1:g.129208A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1134A=	ENSP00000513017.1:p.Pro378=
ENST00000527786.7:c.1113A= MANE Select	ENSP00000433488.2:p.Pro371=
ENST00000281428.12:c.915A=	ENSP00000281428.8:p.Pro305=
ENST00000344954.10:c.534A=	ENSP00000339627.7:p.Pro178=
ENST00000429175.7:c.*1035A=	ENSP00000399985.3:n.*1035A=
ENST00000527786.6:c.1113A=	ENSP00000433488.2:p.Pro371=
ENST00000528790.1:n.3696A=
ENST00000534087.3:c.1014A=	ENSP00000432950.1:p.Pro338=
ENST00000608303.5:c.*505A=	ENSP00000477262.1:n.*505A=
NM_001167681.2:c.1014A=	NP_001161153.1:p.Pro338=
NM_001271010.1:c.915A=	NP_001257939.1:p.Pro305=
NM_001271012.1:c.534A=	NP_001257941.1:p.Pro178=
NM_002017.4:c.1113A=	NP_002008.2:p.Pro371=
XM_011542701.1:c.1014A=	XP_011541003.1:p.Pro338=
XM_011542702.1:c.987A=	XP_011541004.1:p.Pro329=
XM_011542701.2:c.1014A=	XP_011541003.1:p.Pro338=
XM_017017405.1:c.1014A=	XP_016872894.1:p.Pro338=
XM_017017406.1:c.1014A=	XP_016872895.1:p.Pro338=
NM_002017.5:c.1113A= MANE Select	NP_002008.2:p.Pro371=
NM_001167681.3:c.1014A=	NP_001161153.1:p.Pro338=
NM_001271010.2:c.915A=	NP_001257939.1:p.Pro305=
NM_001271012.2:c.534A=	NP_001257941.1:p.Pro178=