Canonical Allele Identifier: CA477702612

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680535G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810640G>T , CM000673.2:g.128810640G>T	GRCh38
NC_000011.9:g.128680535G>T , CM000673.1:g.128680535G>T	GRCh37
NC_000011.8:g.128185745G>T	NCBI36
NG_032912.1:g.129106G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1032G>T	ENSP00000513017.1:p.Arg344=
ENST00000527786.7:c.1011G>T MANE Select	ENSP00000433488.2:p.Arg337=
ENST00000281428.12:c.813G>T	ENSP00000281428.8:p.Arg271=
ENST00000344954.10:c.432G>T	ENSP00000339627.7:p.Arg144=
ENST00000429175.7:c.*933G>T	ENSP00000399985.3:n.*933G>T
ENST00000527786.6:c.1011G>T	ENSP00000433488.2:p.Arg337=
ENST00000528790.1:n.3594G>T
ENST00000534087.3:c.912G>T	ENSP00000432950.1:p.Arg304=
ENST00000608303.5:c.*403G>T	ENSP00000477262.1:n.*403G>T
NM_001167681.2:c.912G>T	NP_001161153.1:p.Arg304=
NM_001271010.1:c.813G>T	NP_001257939.1:p.Arg271=
NM_001271012.1:c.432G>T	NP_001257941.1:p.Arg144=
NM_002017.4:c.1011G>T	NP_002008.2:p.Arg337=
XM_011542701.1:c.912G>T	XP_011541003.1:p.Arg304=
XM_011542702.1:c.885G>T	XP_011541004.1:p.Arg295=
XM_011542701.2:c.912G>T	XP_011541003.1:p.Arg304=
XM_017017405.1:c.912G>T	XP_016872894.1:p.Arg304=
XM_017017406.1:c.912G>T	XP_016872895.1:p.Arg304=
NM_002017.5:c.1011G>T MANE Select	NP_002008.2:p.Arg337=
NM_001167681.3:c.912G>T	NP_001161153.1:p.Arg304=
NM_001271010.2:c.813G>T	NP_001257939.1:p.Arg271=
NM_001271012.2:c.432G>T	NP_001257941.1:p.Arg144=