Canonical Allele Identifier: CA477702253

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680355A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810460A>G , CM000673.2:g.128810460A>G	GRCh38
NC_000011.9:g.128680355A>G , CM000673.1:g.128680355A>G	GRCh37
NC_000011.8:g.128185565A>G	NCBI36
NG_032912.1:g.128926A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.852A>G	ENSP00000513017.1:p.Gly284=
ENST00000527786.7:c.831A>G MANE Select	ENSP00000433488.2:p.Gly277=
ENST00000281428.12:c.633A>G	ENSP00000281428.8:p.Gly211=
ENST00000344954.10:c.252A>G	ENSP00000339627.7:p.Gly84=
ENST00000429175.7:c.*753A>G	ENSP00000399985.3:n.*753A>G
ENST00000527786.6:c.831A>G	ENSP00000433488.2:p.Gly277=
ENST00000528790.1:n.3414A>G
ENST00000534087.3:c.732A>G	ENSP00000432950.1:p.Gly244=
ENST00000608303.5:c.*223A>G	ENSP00000477262.1:n.*223A>G
NM_001167681.2:c.732A>G	NP_001161153.1:p.Gly244=
NM_001271010.1:c.633A>G	NP_001257939.1:p.Gly211=
NM_001271012.1:c.252A>G	NP_001257941.1:p.Gly84=
NM_002017.4:c.831A>G	NP_002008.2:p.Gly277=
XM_011542701.1:c.732A>G	XP_011541003.1:p.Gly244=
XM_011542702.1:c.705A>G	XP_011541004.1:p.Gly235=
XM_011542701.2:c.732A>G	XP_011541003.1:p.Gly244=
XM_017017405.1:c.732A>G	XP_016872894.1:p.Gly244=
XM_017017406.1:c.732A>G	XP_016872895.1:p.Gly244=
NM_002017.5:c.831A>G MANE Select	NP_002008.2:p.Gly277=
NM_001167681.3:c.732A>G	NP_001161153.1:p.Gly244=
NM_001271010.2:c.633A>G	NP_001257939.1:p.Gly211=
NM_001271012.2:c.252A>G	NP_001257941.1:p.Gly84=