Canonical Allele Identifier: CA383238940

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680579A>C (hg19) ; chr11:g.128810684A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810684A>C , CM000673.2:g.128810684A>C	GRCh38
NC_000011.9:g.128680579A>C , CM000673.1:g.128680579A>C	GRCh37
NC_000011.8:g.128185789A>C	NCBI36
NG_032912.1:g.129150A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1076A>C	ENSP00000513017.1:p.His359Pro
ENST00000527786.7:c.1055A>C MANE Select	ENSP00000433488.2:p.His352Pro
ENST00000281428.12:c.857A>C	ENSP00000281428.8:p.His286Pro
ENST00000344954.10:c.476A>C	ENSP00000339627.7:p.His159Pro
ENST00000429175.7:c.*977A>C	ENSP00000399985.3:n.*977A>C
ENST00000527786.6:c.1055A>C	ENSP00000433488.2:p.His352Pro
ENST00000528790.1:n.3638A>C
ENST00000534087.3:c.956A>C	ENSP00000432950.1:p.His319Pro
ENST00000608303.5:c.*447A>C	ENSP00000477262.1:n.*447A>C
NM_001167681.2:c.956A>C	NP_001161153.1:p.His319Pro
NM_001271010.1:c.857A>C	NP_001257939.1:p.His286Pro
NM_001271012.1:c.476A>C	NP_001257941.1:p.His159Pro
NM_002017.4:c.1055A>C	NP_002008.2:p.His352Pro
XM_011542701.1:c.956A>C	XP_011541003.1:p.His319Pro
XM_011542702.1:c.929A>C	XP_011541004.1:p.His310Pro
XM_011542701.2:c.956A>C	XP_011541003.1:p.His319Pro
XM_017017405.1:c.956A>C	XP_016872894.1:p.His319Pro
XM_017017406.1:c.956A>C	XP_016872895.1:p.His319Pro
NM_002017.5:c.1055A>C MANE Select	NP_002008.2:p.His352Pro
NM_001167681.3:c.956A>C	NP_001161153.1:p.His319Pro
NM_001271010.2:c.857A>C	NP_001257939.1:p.His286Pro
NM_001271012.2:c.476A>C	NP_001257941.1:p.His159Pro