Canonical Allele Identifier: CA477702601

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680508C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810613C>G , CM000673.2:g.128810613C>G	GRCh38
NC_000011.9:g.128680508C>G , CM000673.1:g.128680508C>G	GRCh37
NC_000011.8:g.128185718C>G	NCBI36
NG_032912.1:g.129079C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1005C>G	ENSP00000513017.1:p.Pro335=
ENST00000527786.7:c.984C>G MANE Select	ENSP00000433488.2:p.Pro328=
ENST00000281428.12:c.786C>G	ENSP00000281428.8:p.Pro262=
ENST00000344954.10:c.405C>G	ENSP00000339627.7:p.Pro135=
ENST00000429175.7:c.*906C>G	ENSP00000399985.3:n.*906C>G
ENST00000527786.6:c.984C>G	ENSP00000433488.2:p.Pro328=
ENST00000528790.1:n.3567C>G
ENST00000534087.3:c.885C>G	ENSP00000432950.1:p.Pro295=
ENST00000608303.5:c.*376C>G	ENSP00000477262.1:n.*376C>G
NM_001167681.2:c.885C>G	NP_001161153.1:p.Pro295=
NM_001271010.1:c.786C>G	NP_001257939.1:p.Pro262=
NM_001271012.1:c.405C>G	NP_001257941.1:p.Pro135=
NM_002017.4:c.984C>G	NP_002008.2:p.Pro328=
XM_011542701.1:c.885C>G	XP_011541003.1:p.Pro295=
XM_011542702.1:c.858C>G	XP_011541004.1:p.Pro286=
XM_011542701.2:c.885C>G	XP_011541003.1:p.Pro295=
XM_017017405.1:c.885C>G	XP_016872894.1:p.Pro295=
XM_017017406.1:c.885C>G	XP_016872895.1:p.Pro295=
NM_002017.5:c.984C>G MANE Select	NP_002008.2:p.Pro328=
NM_001167681.3:c.885C>G	NP_001161153.1:p.Pro295=
NM_001271010.2:c.786C>G	NP_001257939.1:p.Pro262=
NM_001271012.2:c.405C>G	NP_001257941.1:p.Pro135=