Canonical Allele Identifier: CA477702634

Gene: FLI1

Linked Data

• dbSNP Id: rs1191071402
• MyVariant Identifiers: chr11:g.128680577G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810682G>A , CM000673.2:g.128810682G>A	GRCh38
NC_000011.9:g.128680577G>A , CM000673.1:g.128680577G>A	GRCh37
NC_000011.8:g.128185787G>A	NCBI36
NG_032912.1:g.129148G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1074G>A	ENSP00000513017.1:p.Val358=
ENST00000527786.7:c.1053G>A MANE Select	ENSP00000433488.2:p.Val351=
ENST00000281428.12:c.855G>A	ENSP00000281428.8:p.Val285=
ENST00000344954.10:c.474G>A	ENSP00000339627.7:p.Val158=
ENST00000429175.7:c.*975G>A	ENSP00000399985.3:n.*975G>A
ENST00000527786.6:c.1053G>A	ENSP00000433488.2:p.Val351=
ENST00000528790.1:n.3636G>A
ENST00000534087.3:c.954G>A	ENSP00000432950.1:p.Val318=
ENST00000608303.5:c.*445G>A	ENSP00000477262.1:n.*445G>A
NM_001167681.2:c.954G>A	NP_001161153.1:p.Val318=
NM_001271010.1:c.855G>A	NP_001257939.1:p.Val285=
NM_001271012.1:c.474G>A	NP_001257941.1:p.Val158=
NM_002017.4:c.1053G>A	NP_002008.2:p.Val351=
XM_011542701.1:c.954G>A	XP_011541003.1:p.Val318=
XM_011542702.1:c.927G>A	XP_011541004.1:p.Val309=
XM_011542701.2:c.954G>A	XP_011541003.1:p.Val318=
XM_017017405.1:c.954G>A	XP_016872894.1:p.Val318=
XM_017017406.1:c.954G>A	XP_016872895.1:p.Val318=
NM_002017.5:c.1053G>A MANE Select	NP_002008.2:p.Val351=
NM_001167681.3:c.954G>A	NP_001161153.1:p.Val318=
NM_001271010.2:c.855G>A	NP_001257939.1:p.Val285=
NM_001271012.2:c.474G>A	NP_001257941.1:p.Val158=