Canonical Allele Identifier: CA383238679

Gene: FLI1

Linked Data

• gnomAD v3: 11-128810572-G-T
• gnomAD v4: 11-128810572-G-T
• MyVariant Identifiers: chr11:g.128680467G>T (hg19) ; chr11:g.128810572G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810572G>T , CM000673.2:g.128810572G>T	GRCh38
NC_000011.9:g.128680467G>T , CM000673.1:g.128680467G>T	GRCh37
NC_000011.8:g.128185677G>T	NCBI36
NG_032912.1:g.129038G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.964G>T	ENSP00000513017.1:p.Asp322Tyr
ENST00000527786.7:c.943G>T MANE Select	ENSP00000433488.2:p.Asp315Tyr
ENST00000281428.12:c.745G>T	ENSP00000281428.8:p.Asp249Tyr
ENST00000344954.10:c.364G>T	ENSP00000339627.7:p.Asp122Tyr
ENST00000429175.7:c.*865G>T	ENSP00000399985.3:n.*865G>T
ENST00000527786.6:c.943G>T	ENSP00000433488.2:p.Asp315Tyr
ENST00000528790.1:n.3526G>T
ENST00000534087.3:c.844G>T	ENSP00000432950.1:p.Asp282Tyr
ENST00000608303.5:c.*335G>T	ENSP00000477262.1:n.*335G>T
NM_001167681.2:c.844G>T	NP_001161153.1:p.Asp282Tyr
NM_001271010.1:c.745G>T	NP_001257939.1:p.Asp249Tyr
NM_001271012.1:c.364G>T	NP_001257941.1:p.Asp122Tyr
NM_002017.4:c.943G>T	NP_002008.2:p.Asp315Tyr
XM_011542701.1:c.844G>T	XP_011541003.1:p.Asp282Tyr
XM_011542702.1:c.817G>T	XP_011541004.1:p.Asp273Tyr
XM_011542701.2:c.844G>T	XP_011541003.1:p.Asp282Tyr
XM_017017405.1:c.844G>T	XP_016872894.1:p.Asp282Tyr
XM_017017406.1:c.844G>T	XP_016872895.1:p.Asp282Tyr
NM_002017.5:c.943G>T MANE Select	NP_002008.2:p.Asp315Tyr
NM_001167681.3:c.844G>T	NP_001161153.1:p.Asp282Tyr
NM_001271010.2:c.745G>T	NP_001257939.1:p.Asp249Tyr
NM_001271012.2:c.364G>T	NP_001257941.1:p.Asp122Tyr