Canonical Allele Identifier: CA383238734

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680491G>T (hg19) ; chr11:g.128810596G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810596G>T , CM000673.2:g.128810596G>T	GRCh38
NC_000011.9:g.128680491G>T , CM000673.1:g.128680491G>T	GRCh37
NC_000011.8:g.128185701G>T	NCBI36
NG_032912.1:g.129062G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.988G>T	ENSP00000513017.1:p.Glu330Ter
ENST00000527786.7:c.967G>T MANE Select	ENSP00000433488.2:p.Glu323Ter
ENST00000281428.12:c.769G>T	ENSP00000281428.8:p.Glu257Ter
ENST00000344954.10:c.388G>T	ENSP00000339627.7:p.Glu130Ter
ENST00000429175.7:c.*889G>T	ENSP00000399985.3:n.*889G>T
ENST00000527786.6:c.967G>T	ENSP00000433488.2:p.Glu323Ter
ENST00000528790.1:n.3550G>T
ENST00000534087.3:c.868G>T	ENSP00000432950.1:p.Glu290Ter
ENST00000608303.5:c.*359G>T	ENSP00000477262.1:n.*359G>T
NM_001167681.2:c.868G>T	NP_001161153.1:p.Glu290Ter
NM_001271010.1:c.769G>T	NP_001257939.1:p.Glu257Ter
NM_001271012.1:c.388G>T	NP_001257941.1:p.Glu130Ter
NM_002017.4:c.967G>T	NP_002008.2:p.Glu323Ter
XM_011542701.1:c.868G>T	XP_011541003.1:p.Glu290Ter
XM_011542702.1:c.841G>T	XP_011541004.1:p.Glu281Ter
XM_011542701.2:c.868G>T	XP_011541003.1:p.Glu290Ter
XM_017017405.1:c.868G>T	XP_016872894.1:p.Glu290Ter
XM_017017406.1:c.868G>T	XP_016872895.1:p.Glu290Ter
NM_002017.5:c.967G>T MANE Select	NP_002008.2:p.Glu323Ter
NM_001167681.3:c.868G>T	NP_001161153.1:p.Glu290Ter
NM_001271010.2:c.769G>T	NP_001257939.1:p.Glu257Ter
NM_001271012.2:c.388G>T	NP_001257941.1:p.Glu130Ter