Canonical Allele Identifier: CA16621536

Gene: FLI1

Linked Data

• ClinVar Variation Id: 424635
• ClinVar RCV Id: RCV000487465 ; RCV000851630 ; RCV001821405
• dbSNP Id: rs1064797086
• MyVariant Identifiers: chr11:g.128680534G>A (hg19) ; chr11:g.128810639G>A (hg38)
• PubMed: PMID:28255014

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810639G>A , CM000673.2:g.128810639G>A	GRCh38
NC_000011.9:g.128680534G>A , CM000673.1:g.128680534G>A	GRCh37
NC_000011.8:g.128185744G>A	NCBI36
NG_032912.1:g.129105G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1031G>A	ENSP00000513017.1:p.Arg344Gln
ENST00000527786.7:c.1010G>A MANE Select	ENSP00000433488.2:p.Arg337Gln
ENST00000281428.12:c.812G>A	ENSP00000281428.8:p.Arg271Gln
ENST00000344954.10:c.431G>A	ENSP00000339627.7:p.Arg144Gln
ENST00000429175.7:c.*932G>A	ENSP00000399985.3:n.*932G>A
ENST00000527786.6:c.1010G>A	ENSP00000433488.2:p.Arg337Gln
ENST00000528790.1:n.3593G>A
ENST00000534087.3:c.911G>A	ENSP00000432950.1:p.Arg304Gln
ENST00000608303.5:c.*402G>A	ENSP00000477262.1:n.*402G>A
NM_001167681.2:c.911G>A	NP_001161153.1:p.Arg304Gln
NM_001271010.1:c.812G>A	NP_001257939.1:p.Arg271Gln
NM_001271012.1:c.431G>A	NP_001257941.1:p.Arg144Gln
NM_002017.4:c.1010G>A	NP_002008.2:p.Arg337Gln
XM_011542701.1:c.911G>A	XP_011541003.1:p.Arg304Gln
XM_011542702.1:c.884G>A	XP_011541004.1:p.Arg295Gln
XM_011542701.2:c.911G>A	XP_011541003.1:p.Arg304Gln
XM_017017405.1:c.911G>A	XP_016872894.1:p.Arg304Gln
XM_017017406.1:c.911G>A	XP_016872895.1:p.Arg304Gln
NM_002017.5:c.1010G>A MANE Select	NP_002008.2:p.Arg337Gln
NM_001167681.3:c.911G>A	NP_001161153.1:p.Arg304Gln
NM_001271010.2:c.812G>A	NP_001257939.1:p.Arg271Gln
NM_001271012.2:c.431G>A	NP_001257941.1:p.Arg144Gln