Canonical Allele Identifier: CA383239084

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680641C>A (hg19) ; chr11:g.128810746C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810746C>A , CM000673.2:g.128810746C>A	GRCh38
NC_000011.9:g.128680641C>A , CM000673.1:g.128680641C>A	GRCh37
NC_000011.8:g.128185851C>A	NCBI36
NG_032912.1:g.129212C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1138C>A	ENSP00000513017.1:p.Pro380Thr
ENST00000527786.7:c.1117C>A MANE Select	ENSP00000433488.2:p.Pro373Thr
ENST00000281428.12:c.919C>A	ENSP00000281428.8:p.Pro307Thr
ENST00000344954.10:c.538C>A	ENSP00000339627.7:p.Pro180Thr
ENST00000429175.7:c.*1039C>A	ENSP00000399985.3:n.*1039C>A
ENST00000527786.6:c.1117C>A	ENSP00000433488.2:p.Pro373Thr
ENST00000528790.1:n.3700C>A
ENST00000534087.3:c.1018C>A	ENSP00000432950.1:p.Pro340Thr
ENST00000608303.5:c.*509C>A	ENSP00000477262.1:n.*509C>A
NM_001167681.2:c.1018C>A	NP_001161153.1:p.Pro340Thr
NM_001271010.1:c.919C>A	NP_001257939.1:p.Pro307Thr
NM_001271012.1:c.538C>A	NP_001257941.1:p.Pro180Thr
NM_002017.4:c.1117C>A	NP_002008.2:p.Pro373Thr
XM_011542701.1:c.1018C>A	XP_011541003.1:p.Pro340Thr
XM_011542702.1:c.991C>A	XP_011541004.1:p.Pro331Thr
XM_011542701.2:c.1018C>A	XP_011541003.1:p.Pro340Thr
XM_017017405.1:c.1018C>A	XP_016872894.1:p.Pro340Thr
XM_017017406.1:c.1018C>A	XP_016872895.1:p.Pro340Thr
NM_002017.5:c.1117C>A MANE Select	NP_002008.2:p.Pro373Thr
NM_001167681.3:c.1018C>A	NP_001161153.1:p.Pro340Thr
NM_001271010.2:c.919C>A	NP_001257939.1:p.Pro307Thr
NM_001271012.2:c.538C>A	NP_001257941.1:p.Pro180Thr