Canonical Allele Identifier: CA383239028

Gene: FLI1

Linked Data

• gnomAD v4: 11-128810719-G-T
• MyVariant Identifiers: chr11:g.128680614G>T (hg19) ; chr11:g.128810719G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810719G>T , CM000673.2:g.128810719G>T	GRCh38
NC_000011.9:g.128680614G>T , CM000673.1:g.128680614G>T	GRCh37
NC_000011.8:g.128185824G>T	NCBI36
NG_032912.1:g.129185G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1111G>T	ENSP00000513017.1:p.Gly371Cys
ENST00000527786.7:c.1090G>T MANE Select	ENSP00000433488.2:p.Gly364Cys
ENST00000281428.12:c.892G>T	ENSP00000281428.8:p.Gly298Cys
ENST00000344954.10:c.511G>T	ENSP00000339627.7:p.Gly171Cys
ENST00000429175.7:c.*1012G>T	ENSP00000399985.3:n.*1012G>T
ENST00000527786.6:c.1090G>T	ENSP00000433488.2:p.Gly364Cys
ENST00000528790.1:n.3673G>T
ENST00000534087.3:c.991G>T	ENSP00000432950.1:p.Gly331Cys
ENST00000608303.5:c.*482G>T	ENSP00000477262.1:n.*482G>T
NM_001167681.2:c.991G>T	NP_001161153.1:p.Gly331Cys
NM_001271010.1:c.892G>T	NP_001257939.1:p.Gly298Cys
NM_001271012.1:c.511G>T	NP_001257941.1:p.Gly171Cys
NM_002017.4:c.1090G>T	NP_002008.2:p.Gly364Cys
XM_011542701.1:c.991G>T	XP_011541003.1:p.Gly331Cys
XM_011542702.1:c.964G>T	XP_011541004.1:p.Gly322Cys
XM_011542701.2:c.991G>T	XP_011541003.1:p.Gly331Cys
XM_017017405.1:c.991G>T	XP_016872894.1:p.Gly331Cys
XM_017017406.1:c.991G>T	XP_016872895.1:p.Gly331Cys
NM_002017.5:c.1090G>T MANE Select	NP_002008.2:p.Gly364Cys
NM_001167681.3:c.991G>T	NP_001161153.1:p.Gly331Cys
NM_001271010.2:c.892G>T	NP_001257939.1:p.Gly298Cys
NM_001271012.2:c.511G>T	NP_001257941.1:p.Gly171Cys