Canonical Allele Identifier: CA477702724

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680691T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810796T>C , CM000673.2:g.128810796T>C	GRCh38
NC_000011.9:g.128680691T>C , CM000673.1:g.128680691T>C	GRCh37
NC_000011.8:g.128185901T>C	NCBI36
NG_032912.1:g.129262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1188T>C	ENSP00000513017.1:p.Pro396=
ENST00000527786.7:c.1167T>C MANE Select	ENSP00000433488.2:p.Pro389=
ENST00000281428.12:c.969T>C	ENSP00000281428.8:p.Pro323=
ENST00000344954.10:c.588T>C	ENSP00000339627.7:p.Pro196=
ENST00000429175.7:c.*1089T>C	ENSP00000399985.3:n.*1089T>C
ENST00000527786.6:c.1167T>C	ENSP00000433488.2:p.Pro389=
ENST00000528790.1:n.3750T>C
ENST00000534087.3:c.1068T>C	ENSP00000432950.1:p.Pro356=
ENST00000608303.5:c.*559T>C	ENSP00000477262.1:n.*559T>C
NM_001167681.2:c.1068T>C	NP_001161153.1:p.Pro356=
NM_001271010.1:c.969T>C	NP_001257939.1:p.Pro323=
NM_001271012.1:c.588T>C	NP_001257941.1:p.Pro196=
NM_002017.4:c.1167T>C	NP_002008.2:p.Pro389=
XM_011542701.1:c.1068T>C	XP_011541003.1:p.Pro356=
XM_011542702.1:c.1041T>C	XP_011541004.1:p.Pro347=
XM_011542701.2:c.1068T>C	XP_011541003.1:p.Pro356=
XM_017017405.1:c.1068T>C	XP_016872894.1:p.Pro356=
XM_017017406.1:c.1068T>C	XP_016872895.1:p.Pro356=
NM_002017.5:c.1167T>C MANE Select	NP_002008.2:p.Pro389=
NM_001167681.3:c.1068T>C	NP_001161153.1:p.Pro356=
NM_001271010.2:c.969T>C	NP_001257939.1:p.Pro323=
NM_001271012.2:c.588T>C	NP_001257941.1:p.Pro196=