Canonical Allele Identifier: CA2008247846

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810177C= , CM000673.2:g.128810177C=	GRCh38
NC_000011.9:g.128680072C= , CM000673.1:g.128680072C=	GRCh37
NC_000011.8:g.128185282C=	NCBI36
NG_032912.1:g.128643C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.851-282C=	ENSP00000513017.1:n.851-282C=
ENST00000527786.7:c.830-282C= MANE Select	ENSP00000433488.2:n.830-282C=
ENST00000281428.12:c.632-282C=	ENSP00000281428.8:n.632-282C=
ENST00000344954.10:c.251-282C=	ENSP00000339627.7:n.251-282C=
ENST00000429175.7:c.*752-282C=	ENSP00000399985.3:n.*752-282C=
ENST00000527786.6:c.830-282C=	ENSP00000433488.2:n.830-282C=
ENST00000528790.1:n.3413-282C=
ENST00000534087.3:c.731-282C=	ENSP00000432950.1:n.731-282C=
ENST00000608303.5:c.*222-282C=	ENSP00000477262.1:n.*222-282C=
NM_001167681.2:c.731-282C=	NP_001161153.1:n.731-282C=
NM_001271010.1:c.632-282C=	NP_001257939.1:n.632-282C=
NM_001271012.1:c.251-282C=	NP_001257941.1:n.251-282C=
NM_002017.4:c.830-282C=	NP_002008.2:n.830-282C=
XM_011542701.1:c.731-282C=	XP_011541003.1:n.731-282C=
XM_011542702.1:c.704-282C=	XP_011541004.1:n.704-282C=
XM_011542701.2:c.731-282C=	XP_011541003.1:n.731-282C=
XM_017017405.1:c.731-282C=	XP_016872894.1:n.731-282C=
XM_017017406.1:c.731-282C=	XP_016872895.1:n.731-282C=
NM_002017.5:c.830-282C= MANE Select	NP_002008.2:n.830-282C=
NM_001167681.3:c.731-282C=	NP_001161153.1:n.731-282C=
NM_001271010.2:c.632-282C=	NP_001257939.1:n.632-282C=
NM_001271012.2:c.251-282C=	NP_001257941.1:n.251-282C=