Canonical Allele Identifier: CA477702713

Gene: FLI1

Linked Data

• gnomAD v4: 11-128810784-C-T
• MyVariant Identifiers: chr11:g.128680679C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810784C>T , CM000673.2:g.128810784C>T	GRCh38
NC_000011.9:g.128680679C>T , CM000673.1:g.128680679C>T	GRCh37
NC_000011.8:g.128185889C>T	NCBI36
NG_032912.1:g.129250C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1176C>T	ENSP00000513017.1:p.Ile392=
ENST00000527786.7:c.1155C>T MANE Select	ENSP00000433488.2:p.Ile385=
ENST00000281428.12:c.957C>T	ENSP00000281428.8:p.Ile319=
ENST00000344954.10:c.576C>T	ENSP00000339627.7:p.Ile192=
ENST00000429175.7:c.*1077C>T	ENSP00000399985.3:n.*1077C>T
ENST00000527786.6:c.1155C>T	ENSP00000433488.2:p.Ile385=
ENST00000528790.1:n.3738C>T
ENST00000534087.3:c.1056C>T	ENSP00000432950.1:p.Ile352=
ENST00000608303.5:c.*547C>T	ENSP00000477262.1:n.*547C>T
NM_001167681.2:c.1056C>T	NP_001161153.1:p.Ile352=
NM_001271010.1:c.957C>T	NP_001257939.1:p.Ile319=
NM_001271012.1:c.576C>T	NP_001257941.1:p.Ile192=
NM_002017.4:c.1155C>T	NP_002008.2:p.Ile385=
XM_011542701.1:c.1056C>T	XP_011541003.1:p.Ile352=
XM_011542702.1:c.1029C>T	XP_011541004.1:p.Ile343=
XM_011542701.2:c.1056C>T	XP_011541003.1:p.Ile352=
XM_017017405.1:c.1056C>T	XP_016872894.1:p.Ile352=
XM_017017406.1:c.1056C>T	XP_016872895.1:p.Ile352=
NM_002017.5:c.1155C>T MANE Select	NP_002008.2:p.Ile385=
NM_001167681.3:c.1056C>T	NP_001161153.1:p.Ile352=
NM_001271010.2:c.957C>T	NP_001257939.1:p.Ile319=
NM_001271012.2:c.576C>T	NP_001257941.1:p.Ile192=